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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

250 related items for PubMed ID: 21845785

  • 1. Effective date of requirement for premarket approval for three class III preamendments devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2011 Aug 16; 76(158):50663-7. PubMed ID: 21845785
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  • 2. Medical devices; effective date of requirement for premarket approval for three class III preamendments devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Jun 23; 69(120):34917-20. PubMed ID: 15224687
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  • 7. Medical devices; effective date of requirement for premarket approval for three preamendment class III devices. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 13; 65(72):19833-4. PubMed ID: 11010634
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  • 11. Medical devices; retention in class III and effective date of requirement for premarket approval for three preamendments class III devices--FDA. Proposed rule; opportunity to request a change in classification.
    Fed Regist; 1998 Jul 30; 63(146):40673-7. PubMed ID: 10181520
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  • 16. 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
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  • 19. 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
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  • 20. 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
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