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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 35438741)

  • 1. Manufacturer Ordered to Raise Awareness of Recalled Medical Devices.
    Rubin R
    JAMA; 2022 Apr; 327(15):1439. PubMed ID: 35438741
    [No Abstract]   [Full Text] [Related]  

  • 2. Recalls and Premarket Review Systems for High-Risk Medical Devices in Japan.
    Nakayama M; Tanaka S; Hamada S; Uchida T; Kawakami K
    Ther Innov Regul Sci; 2019 Nov; 53(6):775-780. PubMed ID: 30526015
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Software-Related Recalls of Health Information Technology and Other Medical Devices: Implications for FDA Regulation of Digital Health.
    Ronquillo JG; Zuckerman DM
    Milbank Q; 2017 Sep; 95(3):535-553. PubMed ID: 28895231
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Petition of European experts on medical products legislation].
    Z Evid Fortbild Qual Gesundhwes; 2013; 107(4-5):347-50. PubMed ID: 24066377
    [No Abstract]   [Full Text] [Related]  

  • 5. US Congress considers new tracking system for medical devices after excessive recalls.
    Epstein K
    BMJ; 2012 Apr; 344():e2915. PubMed ID: 22529316
    [No Abstract]   [Full Text] [Related]  

  • 6. Research: Evaluation of Orthopedic Hip Device Recalls by the FDA from 2007 to 2017.
    Peters W; Pellerin C; Janney C
    Biomed Instrum Technol; 2020 Nov; 54(6):418-426. PubMed ID: 33339030
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assessment of cardiovascular and noncardiovascular medical device recalls.
    Somberg JC; McEwen P; Molnar J
    Am J Cardiol; 2014 Jun; 113(11):1899-903. PubMed ID: 24837271
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Assessment of Obstetric and Gynecologic Food and Drug Administration Device Approvals and Recalls.
    Galhotra S; Maurice J
    J Minim Invasive Gynecol; 2018; 25(7):1281-1288. PubMed ID: 29653261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
    Janetos TM; Ghobadi CW; Xu S; Walter JR
    Am J Obstet Gynecol; 2017 Jul; 217(1):42-46.e1. PubMed ID: 28500861
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The FDA and the medical device approval process.
    Guez G; Garg A
    Dent Implantol Update; 2012 May; 23(5):33-7. PubMed ID: 22594003
    [No Abstract]   [Full Text] [Related]  

  • 11. Incremental Revisions across the Life Span of Ophthalmic Devices after Initial Food and Drug Administration Premarket Approval, 1979-2015.
    Gopal AD; Rathi VK; Teng CC; Del Priore L; Ross JS
    Ophthalmology; 2017 Aug; 124(8):1237-1246. PubMed ID: 28501378
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An Oversight in Oversight: Reconciling the Medical Device Industry, Clinicians, and Regulation.
    Landeen KC; Langerman A; Maldonado F
    Chest; 2022 Jan; 161(1):300-302. PubMed ID: 35000707
    [No Abstract]   [Full Text] [Related]  

  • 13. Post-approval studies in France, challenges facing medical devices.
    Levesque K; Coqueblin C; Guillot B; ; Aubourg L; Avouac B; Carbonneil C; Cucherat M; Descamps-Mandine P; Hanoka S; Goldberg M; Josseran A; Parquin F; Pitel S; Ratignier C; Sechoy O; Szwarcenstein K; Tanti A; Teiger E; Thevenet N
    Therapie; 2014; 69(4):303-21. PubMed ID: 25230354
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of FDA-Approved Orthopaedic Devices and Their Recalls.
    Day CS; Park DJ; Rozenshteyn FS; Owusu-Sarpong N; Gonzalez A
    J Bone Joint Surg Am; 2016 Mar; 98(6):517-24. PubMed ID: 26984921
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.
    Connor MJ; Marshall DC; Moiseenko V; Moore K; Cervino L; Atwood T; Sanghvi P; Mundt AJ; Pawlicki T; Recht A; Hattangadi-Gluth JA
    Int J Radiat Oncol Biol Phys; 2017 Jan; 97(1):18-26. PubMed ID: 27979446
    [TBL] [Abstract][Full Text] [Related]  

  • 16. How do Orthopaedic Devices Change After Their Initial FDA Premarket Approval?
    Samuel AM; Rathi VK; Grauer JN; Ross JS
    Clin Orthop Relat Res; 2016 Apr; 474(4):1053-68. PubMed ID: 26584802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MEDICAL DEVICE RECALLS IN CANADA FROM 2005 TO 2015.
    Gagliardi AR; Takata J; Ducey A; Lehoux P; Ross S; Trbovich PL; Easty A; Bell CM; Urbach DR
    Int J Technol Assess Health Care; 2017 Jan; 33(6):708-714. PubMed ID: 28918758
    [TBL] [Abstract][Full Text] [Related]  

  • 18.
    Zhang Y; Masci P; Jones P; Thimbleby H
    Biomed Instrum Technol; 2019; 53(3):182-194. PubMed ID: 31162965
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Medical Device Recalls in Radiation Oncology: Analysis of US Food and Drug Administration Data, 2002-2015.
    Connor MJ; Tringale K; Moiseenko V; Marshall DC; Moore K; Cervino L; Atwood T; Brown D; Mundt AJ; Pawlicki T; Recht A; Hattangadi-Gluth JA
    Int J Radiat Oncol Biol Phys; 2017 Jun; 98(2):438-446. PubMed ID: 28463163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The 510(k) Ancestry of Transvaginal Mesh: When the Subject Is Not a Predicate.
    Rosh J; Bell CM; Urbach DR
    JAMA Surg; 2021 Aug; 156(8):701-702. PubMed ID: 33978687
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.