Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
11 to 16 of 16 Results
ProductCode: FGE Applicant: C.R. BARD, INC. Decision Date To: 02/03/2023
 < 
 1 
 2 
 
Results per Page
New Search  
Export all 16 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
davol retrieval balloon catheter C.R. BARD, INC. K853543 09/20/1985
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
eliminator balloon dilator C.R. BARD, INC. K940965 05/20/1994
lifestent biliary stent system, lifestent xl biliary stent system C.R. BARD, INC. K130792 08/30/2013
luminexx endoscopic biliary stent C.R. BARD, INC. K031186 05/06/2003
usci endoprosthesis C.R. BARD, INC. K834574 04/05/1984
-
-