BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 27207165)

  • 21. An overview of Food and Drug Administration regulation of drugs, biologics, and devices to be used for management of periodontal diseases.
    Tylenda CA; Weintraub M
    Ann Periodontol; 1997 Mar; 2(1):11-7. PubMed ID: 9151539
    [TBL] [Abstract][Full Text] [Related]  

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

  • 23. Dermatologic Device Clearance Within the Food and Drug Administration's 510(k) Pathway.
    Ezaldein HH; Hill ST; Merati M; Suggs A; Reichert B; Scott JF
    Lasers Surg Med; 2020 Nov; 52(9):837-841. PubMed ID: 32221981
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The current situation and development of medical device testing institutes in China.
    Yang X; Mu R; Fan Y; Wang C; Li D
    Expert Rev Med Devices; 2017 Apr; 14(4):263-269. PubMed ID: 28388243
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mapping the genealogy of medical device predicates in the United States.
    Pai DB
    PLoS One; 2021; 16(10):e0258153. PubMed ID: 34618861
    [TBL] [Abstract][Full Text] [Related]  

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

  • 27. US Food and Drug Administration Clearance of Moderate-Risk Otolaryngologic Devices via the 510(k) Process, 1997-2016.
    Rathi VK; Gadkaree SK; Ross JS; Kozin ED; Sethi RK; Naunheim MR; Puram SV; Gray ST
    Otolaryngol Head Neck Surg; 2017 Oct; 157(4):608-617. PubMed ID: 28786317
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Technology assessment of medical devices at the Center for Devices and Radiological Health.
    Kessler L; Richter K
    Am J Manag Care; 1998 Sep; 4 Spec No():SP129-35. PubMed ID: 10185989
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Introduction of innovative high-risk medical devices in Europe: are clinical efficacy and safety guaranteed?].
    Stordeur S; Vinck I; Neyt M; Van Brabandt H; Hulstaert F
    Rev Epidemiol Sante Publique; 2013 Apr; 61(2):105-10. PubMed ID: 23477881
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Assessment of Data Sources That Support US Food and Drug Administration Medical Devices Safety Communications.
    Tau N; Shepshelovich D
    JAMA Intern Med; 2020 Nov; 180(11):1420-1426. PubMed ID: 32986074
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Food and Drug Administration control of medical devices: an inescapable intrusion and stimulus for adaptation.
    Friedman EA
    ASAIO J; 1998; 44(4):239-40. PubMed ID: 9682946
    [No Abstract]   [Full Text] [Related]  

  • 32. Improving medical device regulation: the United States and Europe in perspective.
    Sorenson C; Drummond M
    Milbank Q; 2014 Mar; 92(1):114-50. PubMed ID: 24597558
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Role of the FDA and Regulatory Approval of New Devices for Diabetes Care.
    Jazowski SA; Winn AN
    Curr Diab Rep; 2017 Jun; 17(6):40. PubMed ID: 28439847
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Off-Label Use of Medical Devices in Children.
    ;
    Pediatrics; 2017 Jan; 139(1):. PubMed ID: 28025239
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The regulation of medical devices.
    Wilmshurst P
    BMJ; 2011 May; 342():d2822. PubMed ID: 21572131
    [No Abstract]   [Full Text] [Related]  

  • 36. Time to publication of cost-effectiveness analyses for medical devices.
    Everhart AO
    Am J Manag Care; 2023 May; 29(5):265-268. PubMed ID: 37229785
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Interconnected Ancestral Network of Hip Arthroplasty Device Approval.
    Premkumar A; Zhu A; Ying X; Pean CA; Sheth NP; Cross MB; Gonzalez Della Valle A
    J Am Acad Orthop Surg; 2021 Dec; 29(24):e1362-e1369. PubMed ID: 34161960
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comparison of rates of safety issues and reporting of trial outcomes for medical devices approved in the European Union and United States: cohort study.
    Hwang TJ; Sokolov E; Franklin JM; Kesselheim AS
    BMJ; 2016 Jun; 353():i3323. PubMed ID: 27352914
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Shoulder arthroplasty device clearance: an ancestral network analysis.
    Zhu A; Ying X; Carey EG; Pean CA; Premkumar A; Fu MC; Taylor SA
    J Shoulder Elbow Surg; 2023 Mar; 32(3):671-676. PubMed ID: 36279987
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Median approval times for class III medical devices have been well above statutory deadlines set for FDA and CMS.
    Zinn AM; Allen JC; Hacker CS
    Health Aff (Millwood); 2012 Oct; 31(10):2304-13. PubMed ID: 23048112
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.