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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 16 Results
ProductCode: FGE Applicant: C.R. BARD, INC. Decision Date To: 02/03/2023
 
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usci endoprosthesis C.R. BARD, INC. K834574 04/05/1984
luminexx endoscopic biliary stent C.R. BARD, INC. K031186 05/06/2003
lifestent biliary stent system, lifestent xl biliary stent system C.R. BARD, INC. K130792 08/30/2013
eliminator balloon dilator C.R. BARD, INC. K940965 05/20/1994
duraglide stone removal balloon, model 000635-38, 000646-47, duraglide stone balloon, model 007124-25,007144-45 C.R. BARD, INC. K993892 01/06/2000
davol retrieval balloon catheter C.R. BARD, INC. K853543 09/20/1985
bard/angiomed stents C.R. BARD, INC. K896391 03/29/1990
bard memotherm transhepatic biliary endoprosthesis C.R. BARD, INC. K963782 05/02/1997
bard memotherm flexx biliary stent C.R. BARD, INC. K993392 01/06/2000
bard memotherm endoscopic biliary stent C.R. BARD, INC. K003186 01/09/2001
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