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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

260 related items for PubMed ID: 10275304

  • 21. General hospital and personal use devices; classification of the Apgar timer, lice removal kit, and infusion stand--FDA. Proposed rule.
    Fed Regist; 1998 Mar 10; 63(46):11632-3. PubMed ID: 10177746
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. General hospital and personal use devices: proposed classification of liquid chemical sterilants and general purpose disinfectants--FDA. Proposed rule.
    Fed Regist; 1998 Nov 06; 63(215):59917-21. PubMed ID: 10187388
    [Abstract] [Full Text] [Related]

  • 24. 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]

  • 25. Medical devices; intent to initiate proceedings to establish effective dates of requirement for premarket approval for 31 class III preamendments devices--FDA. Advance notice of proposed rulemaking.
    Fed Regist; 1989 Jan 06; 54(4):550-2. PubMed ID: 10291347
    [Abstract] [Full Text] [Related]

  • 26. Medical devices; general hospital and personal use devices; classification of the filtering facepiece respirator for use by the general public in public health medical emergencies. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Jul 03; 72(127):36360-3. PubMed ID: 17674487
    [Abstract] [Full Text] [Related]

  • 27. Medical devices; refurbishers, rebuilders, reconditioners, servicers, and "as is" remarketers of medical devices; review and revision of compliance policy guides and regulatory requirements; request for comments and information--FDA. Advance notice of proposed rulemaking.
    Fed Regist; 1997 Dec 23; 62(246):67011-3. PubMed ID: 10179309
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. 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]

  • 30. Medical devices; illustrative and designated lists for device tracking--FDA. Final rule and request for comments.
    Fed Regist; 1993 Aug 16; 58(156):43451-5. PubMed ID: 10171508
    [Abstract] [Full Text] [Related]

  • 31. Medical devices; implementation of third party review under the Food and Drug Administration Modernization Act of 1997; emergency processing request under OMB review--FDA. Notice.
    Fed Regist; 1998 May 22; 63(99):28388-91. PubMed ID: 10179874
    [Abstract] [Full Text] [Related]

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

  • 33. 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]

  • 34. Medtronic, Inc.; premarket approval of the Interstim Sacral Nerve Stimulation (SNS) System--FDA. Notice.
    Fed Regist; 1998 Jan 29; 63(19):4457. PubMed ID: 10177327
    [Abstract] [Full Text] [Related]

  • 35. Medical devices; reclassification and codification of the stainless steel suture. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 13; 65(72):19835-6. PubMed ID: 11010635
    [Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. Medical devices; reports of corrections and removals--FDA. Final rule.
    Fed Regist; 1997 May 19; 62(96):27183. PubMed ID: 10167533
    [Abstract] [Full Text] [Related]

  • 38. 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]

  • 39. 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]

  • 40. FDA marketing claims, and the practitioner.
    Runner S.
    J Evid Based Dent Pract; 2006 Mar 29; 6(1):19-23. PubMed ID: 17138391
    [Abstract] [Full Text] [Related]

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