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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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lifestent biliary stent system, lifestent xl biliary stent system C.R. BARD, INC. K130792 08/30/2013
bard luminexx 3 biliary stent and delivery system C.R. BARD, INC. K033497 02/04/2004
luminexx endoscopic biliary stent C.R. BARD, INC. K031186 05/06/2003
bard conformexx biliary stent and delivery system C.R. BARD, INC. K021994 01/02/2003
bard luminexx 6 fr biliary stent and delivery system C.R. BARD, INC. K020682 04/02/2002
bard memotherm endoscopic biliary stent C.R. BARD, INC. K003186 01/09/2001
bard luminexx biliary stent C.R. BARD, INC. K003793 01/05/2001
bard memotherm flexx biliary stent C.R. BARD, INC. K993392 01/06/2000
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
bard memotherm transhepatic biliary endoprosthesis C.R. BARD, INC. K963782 05/02/1997
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