• 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
-
1 to 8 of 8 Results
ProductCode: DRF Applicant: CORDIS WEBSTER, INC. Decision Date To: 11/28/2022
Results per Page
New Search  
Export all 8 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]
cordis webster fixed curve catheters, models d-1124, d-1085 CORDIS WEBSTER, INC. K992965 11/26/1999
cordis webster diagnostic deflectable tip catheter, model d-1078 CORDIS WEBSTER, INC. K991531 10/04/1999
cordis webster ref-star external reference patch, model # d-1210 CORDIS WEBSTER, INC. K982415 08/10/1998
cordis webster ref-star ex surface reference device model's d-1204-01, -02,-03, and -04. CORDIS WEBSTER, INC. K980961 05/28/1998
cordis webster t20 diagnostic deflectable tip catheter CORDIS WEBSTER, INC. K953663 09/18/1996
coridis webster deflectable braided-tip electrode catheter CORDIS WEBSTER, INC. K955817 03/25/1996
cordis wester star catheter CORDIS WEBSTER, INC. K954390 12/21/1995
cordis webster a20 diagnostic deflectable tip catheter CORDIS WEBSTER, INC. K953768 11/22/1995
-
-