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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

685 related items for PubMed ID: 10177504

  • 41. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20558-61. PubMed ID: 10179320
    [Abstract] [Full Text] [Related]

  • 42. Gastroenterology and urology devices; effective date of requirement for premarket approval of the implanted mechanical/hydraulic urinary continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Sep 26; 65(187):57726-32. PubMed ID: 11503643
    [Abstract] [Full Text] [Related]

  • 43. Guidance of FDA's expectations of medical device manufacturers concerning the year 2000 date problem--FDA. Notice.
    Fed Regist; 1998 Jun 24; 63(121):34433-42. PubMed ID: 10180297
    [Abstract] [Full Text] [Related]

  • 44. Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices--FDA. Final rule.
    Fed Regist; 1998 Nov 20; 63(224):64556-88. PubMed ID: 10339052
    [Abstract] [Full Text] [Related]

  • 45. Medical devices; investigational device exemptions--FDA. Final rule.
    Fed Regist; 1998 Nov 23; 63(225):64617-26. PubMed ID: 10338870
    [Abstract] [Full Text] [Related]

  • 46. Dental devices; dental noble metal alloys and dental base metal alloys; designation of special controls. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Aug 23; 69(162):51765-6. PubMed ID: 15329980
    [Abstract] [Full Text] [Related]

  • 47. Medical devices; immunology and microbiology devices; classification of the West Nile Virus IgM capture Elisa assay. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Oct 30; 68(210):61743-5. PubMed ID: 14587527
    [Abstract] [Full Text] [Related]

  • 48. Medical devices; exemptions from premarket notification; surgical lamps--FDA. Notice.
    Fed Regist; 1998 Dec 04; 63(233):67075-6. PubMed ID: 10338882
    [Abstract] [Full Text] [Related]

  • 49. Medical devices; investigational device exemptions--FDA. Proposed rule.
    Fed Regist; 1998 Jul 15; 63(135):38131-8. PubMed ID: 10181246
    [Abstract] [Full Text] [Related]

  • 50. Cardiovascular and neurological devices; reclassification of two embolization devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Dec 29; 69(249):77898-900. PubMed ID: 15624254
    [Abstract] [Full Text] [Related]

  • 51. FDA Modernization Act of 1997: modifications to the list of recognized standards; availability; withdrawal of draft guidance "Use of IEC 60601 standards; medical electrical equipment"--FDA. Notice.
    Fed Regist; 1998 Oct 16; 63(200):55617-30. PubMed ID: 10185835
    [Abstract] [Full Text] [Related]

  • 52. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices), guidance for FDA reviewers and industry; availability--FDA. Notice.
    Fed Regist; 1998 Nov 06; 63(215):60009-10. PubMed ID: 10187389
    [Abstract] [Full Text] [Related]

  • 53. Medical devices; hematology and pathology devices; classification of the Factor V Leiden DNA mutation detection systems devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Mar 16; 69(51):12271-3. PubMed ID: 15025053
    [Abstract] [Full Text] [Related]

  • 54. Form for reporting serious adverse events and product problems with human drug and biological products and devices; availability--FDA. Notice.
    Fed Regist; 1993 Jun 03; 58(105):31596-614. PubMed ID: 10171452
    [Abstract] [Full Text] [Related]

  • 55. Medical devices: classification of the dental sonography device and jaw tracking device. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 02; 68(231):67365-7. PubMed ID: 14651050
    [Abstract] [Full Text] [Related]

  • 56. Medical devices; exemptions from premarket notification; class II devices; vascular tunnelers. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Mar 03; 65(43):11466-7. PubMed ID: 11010650
    [Abstract] [Full Text] [Related]

  • 57. Medical devices; humanitarian use of devices--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Jul 31; 63(147):40825. PubMed ID: 10181716
    [Abstract] [Full Text] [Related]

  • 58. Gastroenterology-urology devices; effective date of requirement for premarket approval of the penile inflatable implant. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 12; 65(71):19650-8. PubMed ID: 11010632
    [Abstract] [Full Text] [Related]

  • 59. Dental devices; effective date of requirement for premarket approval; temporomandibular joint prostheses--FDA. Final rule.
    Fed Regist; 1998 Dec 30; 63(250):71743-6. PubMed ID: 10339055
    [Abstract] [Full Text] [Related]

  • 60. How do regulatory agencies ensure the release of a safe medical device?
    Haggar B.
    Clin Perform Qual Health Care; 1999 Dec 30; 7(2):100-3. PubMed ID: 10747561
    [Abstract] [Full Text] [Related]

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