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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 493 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 
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510(K)
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yomura safety i.v. catheter YOMURA TECHNOLOGIES INC. K112542 02/08/2012
magicath ii Woo Young Medical Co., Ltd. K210929 09/13/2022
i.v. catheter, models: type i, type y, type straight WEIHAI JIERUI MEDICAL PRODUCTS CO., LTD. K083429 08/07/2009
deseret angio guide WARNER-LAMBERT CO. K821577 06/16/1982
multilumen viapic central line catheter WARNER-LAMBERT CO. K861510 06/09/1986
deseret subclavian jugular cath. set WARNER-LAMBERT CO. K822023 07/28/1982
deseret subclavian jugular cath-set WARNER-LAMBERT CO. K833091 11/21/1983
deseret angio-guide large vein cath. WARNER-LAMBERT CO. K833092 11/21/1983
deseret intracath intravenous catheter WARNER-LAMBERT CO. K821372 06/02/1982
deseret subclavian jugular catheter set WARNER-LAMBERT CO. K821371 06/02/1982
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