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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

577 related items for PubMed ID: 10187384

  • 1. Medical devices; exemptions from premarket notification; class II devices--FDA, Final rule.
    Fed Regist; 1998 Nov 03; 63(212):59222-31. PubMed ID: 10187384
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. Medical devices; exemptions from premarket notification and reserved devices; class I--FDA. Notice.
    Fed Regist; 1998 Feb 02; 63(21):5387-93. PubMed ID: 10177333
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Medical devices; exemption from premarket notification requirements; class I devices; technical amendment. Final rule; technical amendment.
    Food and Drug Administration. HHS.
    Fed Regist; 2001 Jul 25; 66(143):38786-819. PubMed ID: 11725800
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Medical Device; exemption from premarket notification; class II devices; pharmacy compounding systems. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Mar 21; 66(55):15796-8. PubMed ID: 11706859
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Hematology and pathology devices; reclassification of the automated differential cell counter. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Jan 14; 67(9):1606-7. PubMed ID: 11800006
    [Abstract] [Full Text] [Related]

  • 11. 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 28; 66(40):12733-4. PubMed ID: 11503864
    [Abstract] [Full Text] [Related]

  • 12. Medical devices; immunology and microbiology devices; classification of the endotoxin assay. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Oct 31; 68(211):62007-8. PubMed ID: 14594019
    [Abstract] [Full Text] [Related]

  • 13. Medical devices; exemptions from premarket notification; class II devices. Final rule.
    Food and drug Administration, HHS.
    Fed Regist; 2001 Nov 15; 66(221):57368-9. PubMed ID: 11776279
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Medical devices; exemption from premarket notification; class II devices; triiodothyronine test system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Oct 18; 65(202):62285-6. PubMed ID: 11503681
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18. 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 08; 65(237):76930-2. PubMed ID: 11503724
    [Abstract] [Full Text] [Related]

  • 19. Medical devices; classification/reclassification of immunohistochemistry reagents and kits--FDA. Final rule.
    Fed Regist; 1998 Jun 03; 63(106):30132-42. PubMed ID: 10179865
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 29.