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PUBMED FOR HANDHELDS

Journal Abstract Search


305 related items for PubMed ID: 24837271

  • 1. Assessment of cardiovascular and noncardiovascular medical device recalls.
    Somberg JC, McEwen P, Molnar J.
    Am J Cardiol; 2014 Jun 01; 113(11):1899-903. PubMed ID: 24837271
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  • 3. Assessment of Obstetric and Gynecologic Food and Drug Administration Device Approvals and Recalls.
    Galhotra S, Maurice J.
    J Minim Invasive Gynecol; 2018 Jun 01; 25(7):1281-1288. PubMed ID: 29653261
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  • 4. 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 01; 474(4):1053-68. PubMed ID: 26584802
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  • 7. 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 01; 54(6):418-426. PubMed ID: 33339030
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  • 8. Recalls of Moderate- and High-Risk Otolaryngologic Devices Approved by the US Food and Drug Administration, 2003-2019.
    Talati IA, Parsa KM, Gao WZ.
    Otolaryngol Head Neck Surg; 2022 Nov 01; 167(5):832-838. PubMed ID: 35290135
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  • 14. 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 01; 217(1):42-46.e1. PubMed ID: 28500861
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  • 15. Premarket clinical evaluation of novel cardiovascular devices: quality analysis of premarket clinical studies submitted to the Food and Drug Administration 2000-2007.
    Kramer DB, Mallis E, Zuckerman BD, Zimmerman BA, Maisel WH.
    Am J Ther; 2010 Jul 01; 17(1):2-7. PubMed ID: 20038828
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  • 16. Major FDA medical device recalls in ophthalmology from 2003 to 2015.
    Talati RK, Gupta AS, Xu S, Ghobadi CW.
    Can J Ophthalmol; 2018 Apr 01; 53(2):98-103. PubMed ID: 29631834
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  • 17. 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 01; 53(6):775-780. PubMed ID: 30526015
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  • 18. 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 28; 353():i3323. PubMed ID: 27352914
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  • 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 01; 98(2):438-446. PubMed ID: 28463163
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  • 20. Orthopaedic Device Approval Through the Premarket Approval Process: A Financial Feasibility Analysis for a Single Center.
    Yang BW, Iorio ML, Day CS.
    J Bone Joint Surg Am; 2017 Mar 15; 99(6):e26. PubMed ID: 28291189
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