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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

415 related items for PubMed ID: 10178430

  • 1. Medical devices; humanitarian use of devices--FDA. Direct final rule.
    Fed Regist; 1998 Apr 17; 63(74):19185-90. PubMed ID: 10178430
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  • 2. Medical devices; humanitarian use of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 17; 63(74):19196-200. PubMed ID: 10178431
    [Abstract] [Full Text] [Related]

  • 3. Medical devices; reports of corrections and removals--FDA. Direct final rule.
    Fed Regist; 1998 Aug 07; 63(152):42229-33. PubMed ID: 10181725
    [Abstract] [Full Text] [Related]

  • 4. Medical devices; establishment registration and device listing for manufacturers and distributors of devices--FDA. Direct final rule.
    Fed Regist; 1998 Sep 29; 63(188):51825-7. PubMed ID: 10185812
    [Abstract] [Full Text] [Related]

  • 5. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May 12; 63(91):26069-77. PubMed ID: 10179334
    [Abstract] [Full Text] [Related]

  • 6. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20530-3. PubMed ID: 10179319
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Removal of regulations regarding certification of drugs composed wholly or partly of insulin--FDA. Direct final rule.
    Fed Regist; 1998 May 13; 63(92):26694-9. PubMed ID: 10179341
    [Abstract] [Full Text] [Related]

  • 9. Medical devices; reports of corrections and removals; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Aug 07; 63(152):42300-4. PubMed ID: 10181727
    [Abstract] [Full Text] [Related]

  • 10. Medical devices; medical device reporting; baseline reports. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 13; 73(115):33692-5. PubMed ID: 18677824
    [Abstract] [Full Text] [Related]

  • 11. Revisions to the general safety requirements for biological products--FD. Direct final rule.
    Fed Regist; 1998 Apr 20; 63(75):19399-403. PubMed ID: 10178869
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  • 13. Investigational new drug applications; clinical holds--FDA. Direct final rule.
    Fed Regist; 1998 Dec 14; 63(239):68676-8. PubMed ID: 10187558
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Medical devices; humanitarian use of devices--FDA. Final rule.
    Fed Regist; 1998 Nov 03; 63(212):59217-22. PubMed ID: 10187383
    [Abstract] [Full Text] [Related]

  • 16. Amendment of various device regulations to reflect current American Society for Testing and Material citations. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Jan 24; 65(15):3584-5. PubMed ID: 11010654
    [Abstract] [Full Text] [Related]

  • 17. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Aug 11; 63(154):42699. PubMed ID: 10182563
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