These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

345 related articles for article (PubMed ID: 11067678)

  • 41. Medical devices; obstetrical and gynecological devices; classification of the breast lesion documentation system. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Jul; 68(144):44413-5. PubMed ID: 12884877
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Cardiovascular devices; reclassification of intra-aortic balloon and control systems for acute coronary syndrome, cardiac and non-cardiac surgery, or complications of heart failure; effective date of requirement for premarket approval for intra-aortic balloon and control systems for septic shock or pulsatile flow generation. Final order.
    Food and Drug Administration, HHS
    Fed Regist; 2013 Dec; 78(250):79300-3. PubMed ID: 24383147
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Effective date of requirement for premarket approval for transilluminator for breast evaluation and sorbent hemoperfusion system (SHS) devices for the treatment of hepatic coma and metabolic disturbances; reclassification of SHS and devices for the treatment of poisoning and drug overdose. Final order.
    Food and Drug Administration, HHS
    Fed Regist; 2014 Jan; 79(12):3088-94. PubMed ID: 24443766
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Cardiovascular, orthopedic, and physical medicine diagnostic devices; reclassification of cardiopulmonary bypass accessory equipment, goniometer device, and electrode cable devices. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr; 65(70):19317-9. PubMed ID: 11010630
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Aug; 63(154):42699. PubMed ID: 10182563
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Medical devices; ear, nose and throat devices; reclassification of the endolymphatic shunt tube with valve. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Apr; 67(82):20893-4. PubMed ID: 11980454
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Medical device; exemption from premarket notification; class II devices; barium enema retention catheters and tips with or without a bag. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Dec; 65(237):76930-2. PubMed ID: 11503724
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Medical Device; exemption from premarket notification; class II devices; pharmacy compounding systems. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2001 Mar; 66(55):15796-8. PubMed ID: 11706859
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Obstetric and gynecologic devices; reclassification and classification of medical devices used for in vitro fertilization and related assisted reproduction procedures--FDA. Final rule.
    Fed Regist; 1998 Sep; 63(175):48428-37. PubMed ID: 10182829
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Neurological Devices; Reclassification of Electroconvulsive Therapy Devices; Effective Date of Requirement for Premarket Approval for Electroconvulsive Therapy Devices for Certain Specified Intended Uses. Final order.
    Food and Drug Administration, HHS
    Fed Regist; 2018 Dec; 83(246):66103-24. PubMed ID: 30596410
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Medical devices; apnea monitor; special controls. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Jul; 67(137):46851-2. PubMed ID: 12125715
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Cardiovascular devices; reclassification of nonroller-type cardiopulmonary bypass blood pumps for cardiopulmonary and circulatory bypass; effective date of requirement for premarket approval for nonroller-type cardiopulmonary bypass blood pumps for temporary ventricular support. Final order.
    Food and Drug Administration, HHS
    Fed Regist; 2015 Jun; 80(109):32307-11. PubMed ID: 26054096
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Medical devices; gastroenterology-urology devices; nonimplanted, peripheral electrical continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr; 65(68):18236-7. PubMed ID: 11010624
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Medical devices; reclassification and codification of vitamin D test system--FDA. Final rule.
    Fed Regist; 1998 Jul; 63(145):40364-6. PubMed ID: 10181714
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Clinical chemistry and clinical toxicology devices; classification of B-type natriuretic peptide test system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2001 Feb; 66(40):12733-4. PubMed ID: 11503864
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Medical devices; pediatric uses of devices; requirement for submission of information on pediatric subpopulations that suffer from a disease or condition that a device is intended to treat, diagnose, or cure; direct final rule. Direct final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2010 Apr; 75(62):16347-51. PubMed ID: 20383921
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Orthopedic devices: reclassification of the hip joint metal/polymer constrained cemented or uncemented prosthesis. Final Rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Apr; 67(83):21171-3. PubMed ID: 11982031
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Supplemental applications proposing labeling changes for approved drugs, biologics, and medical devices. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2008 Aug; 73(164):49603-10. PubMed ID: 18958946
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Medical devices; reports of corrections and removals; lift of stay of effective date--FDA. Final rule; lift of stay of effective date.
    Fed Regist; 1998 Apr; 63(73):18836. PubMed ID: 10179315
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Medical devices; exemptions from premarket notification; class II devices. Final rule.
    Food and drug Administration, HHS
    Fed Regist; 2001 Nov; 66(221):57368-9. PubMed ID: 11776279
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.