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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

243 related items for PubMed ID: 10115560

  • 1. Order for transitional class III devices; submission of safety and effectiveness information under section 520(1)(5)(A) of the Federal Food, Drug, and Cosmetic Act--FDA. Notice.
    Fed Regist; 1991 Nov 14; 56(220):57960-3. PubMed ID: 10115560
    [Abstract] [Full Text] [Related]

  • 2. Medical devices; substantial equivalence; 510(K) summaries and 510(K) statements; class III summaries; confidentiality of information--FDA. Final rule.
    Fed Regist; 1994 Dec 14; 59(239):64287-96. PubMed ID: 10139433
    [Abstract] [Full Text] [Related]

  • 3. Medical devices; gastroenterology and urology devices; classification of the electrogastrography system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Sep 23; 64(184):51442-4. PubMed ID: 11010709
    [Abstract] [Full Text] [Related]

  • 4. Medical devices; gastroenterology-urology devices; nonimplanted, peripheral electrical continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 07; 65(68):18236-7. PubMed ID: 11010624
    [Abstract] [Full Text] [Related]

  • 5. Medical devices; classification/reclassification; restricted devices; analyte specific reagents--FDA. Final rule.
    Fed Regist; 1997 Nov 21; 62(225):62243-60. PubMed ID: 10177056
    [Abstract] [Full Text] [Related]

  • 6. What physicians should know about the regulation of Obstetric and Gynecologic Medical Devices.
    Yin L.
    J Reprod Med; 1983 Jan 21; 28(1):3-11. PubMed ID: 6834344
    [Abstract] [Full Text] [Related]

  • 7. Medical devices; classification for medical washer and medical washer-disinfector. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Nov 15; 67(221):69119-21. PubMed ID: 12437015
    [Abstract] [Full Text] [Related]

  • 8. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 14; 65(10):2296-323. PubMed ID: 11010655
    [Abstract] [Full Text] [Related]

  • 9. Medical devices; device tracking--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
    Fed Regist; 1992 May 29; 57(104):22966-70. PubMed ID: 10171013
    [Abstract] [Full Text] [Related]

  • 10. Orthopedic devices: classification and reclassification of pedicle screw spinal systems--FDA. Final rule.
    Fed Regist; 1998 Jul 27; 63(143):40025-41. PubMed ID: 10181517
    [Abstract] [Full Text] [Related]

  • 11. Medical devices; obstetrical and gynecological devices; classification of the breast lesion documentation system. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jul 28; 68(144):44413-5. PubMed ID: 12884877
    [Abstract] [Full Text] [Related]

  • 12. Medical devices; medical device distributor reporting--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
    Fed Regist; 1993 Sep 01; 58(168):46514-23. PubMed ID: 10128335
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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 29; 67(82):20893-4. PubMed ID: 11980454
    [Abstract] [Full Text] [Related]

  • 15. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10638-40. PubMed ID: 10177504
    [Abstract] [Full Text] [Related]

  • 16. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
    Fed Regist; 1992 Dec 10; 57(238):58400-6. PubMed ID: 10123143
    [Abstract] [Full Text] [Related]

  • 17. Export of pharmaceuticals and medical devices under the federal Food, Drug & Cosmetic Act: FDA's striking change in interpretation post-Shelhigh.
    Basile EM, Tolomeo D, Gluck E.
    Food Drug Law J; 2009 Dec 10; 64(1):149-69. PubMed ID: 19998744
    [Abstract] [Full Text] [Related]

  • 18. Medical devices; exemption from premarket notification and reserved devices; Class I--FDA. Proposed rule.
    Fed Regist; 1998 Nov 12; 63(218):63222-53. PubMed ID: 10187398
    [Abstract] [Full Text] [Related]

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  • 20. Medical devices; reclassification of six cardiovascular preamendments class III devices into class II. Final rule.
    Food and Drug Administration.
    Fed Regist; 2001 Apr 10; 66(69):18540-2. PubMed ID: 11721689
    [Abstract] [Full Text] [Related]

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