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Journal Abstract Search

193 related items for PubMed ID: 36625810

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  • 2. Association Between Regulatory Submission Characteristics and Recalls of Medical Devices Receiving 510(k) Clearance.
    Everhart AO, Sen S, Stern AD, Zhu Y, Karaca-Mandic P.
    JAMA; 2023 Jan 10; 329(2):144-156. PubMed ID: 36625811
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  • 5. 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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  • 6. Risk of Recall Among Medical Devices Undergoing US Food and Drug Administration 510(k) Clearance and Premarket Approval, 2008-2017.
    Dubin JR, Simon SD, Norrell K, Perera J, Gowen J, Cil A.
    JAMA Netw Open; 2021 May 03; 4(5):e217274. PubMed ID: 33956132
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  • 7. Medical device recalls and the FDA approval process.
    Zuckerman DM, Brown P, Nissen SE.
    Arch Intern Med; 2011 Jun 13; 171(11):1006-11. PubMed ID: 21321283
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  • 11. 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 13; 167(5):832-838. PubMed ID: 35290135
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  • 12. Class I Recalls of Cardiovascular Devices Between 2013 and 2022 : A Cross-Sectional Analysis.
    See C, Mooghali M, Dhruva SS, Ross JS, Krumholz HM, Kadakia KT.
    Ann Intern Med; 2024 Nov 13; 177(11):1499-1508. PubMed ID: 39284187
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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 13; 217(1):42-46.e1. PubMed ID: 28500861
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  • 15. 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 13; 124(8):1237-1246. PubMed ID: 28501378
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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 13; 53(6):775-780. PubMed ID: 30526015
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  • 18. The regulatory ancestral network of surgical meshes.
    Zargar N, Carr A.
    PLoS One; 2018 Nov 13; 13(6):e0197883. PubMed ID: 29920525
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  • 19. Major FDA medical device recalls in ophthalmology from 2003 to 2015.
    Talati RK, Gupta AS, Xu S, Ghobadi CW.
    Can J Ophthalmol; 2018 Apr 13; 53(2):98-103. PubMed ID: 29631834
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