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 20 of 22 Results
ProductCode: LJT Applicant: C.R. BARD, INC. Decision Date To: 04/26/2024
 < 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 22 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]
powerport polymetric port with 8 fr s/l chronoflex catheter C.R. BARD, INC. K063377 01/25/2007
powerport(tm)implanted titanium port w/8 fr. chronoflex catheter-multiple C.R. BARD, INC. K060812 07/14/2006
modification to x-port duo port C.R. BARD, INC. K034065 01/15/2004
x-prot duo port C.R. BARD, INC. K032044 07/10/2003
bardport x-port isp port C.R. BARD, INC. K022983 09/25/2002
dual slim port implanted port (0654970/0654940) C.R. BARD, INC. K964066 03/06/1997
hickman plastic subcutaneous port C.R. BARD, INC. K873213 10/27/1987
mediport ii model mp-dl vascular access port C.R. BARD, INC. K870817 07/30/1987
hickman titanium subcutaneous port C.R. BARD, INC. K870260 04/15/1987
mediport ii single lum/port implant vasc acs port C.R. BARD, INC. K864349 02/10/1987
-
-