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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 16 of 16 Results
ProductCode: FGE Applicant: C.R. BARD, INC. Decision Date To: 02/03/2023
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510(K)
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bard memotherm endoscopic biliary stent C.R. BARD, INC. K003186 01/09/2001
bard luminexx 6 fr biliary stent and delivery system C.R. BARD, INC. K020682 04/02/2002
bard conformexx biliary stent and delivery system C.R. BARD, INC. K021994 01/02/2003
luminexx endoscopic biliary stent C.R. BARD, INC. K031186 05/06/2003
bard luminexx 3 biliary stent and delivery system C.R. BARD, INC. K033497 02/04/2004
lifestent biliary stent system, lifestent xl biliary stent system C.R. BARD, INC. K130792 08/30/2013
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