8F LAUNCHER GUIDE CATHETER


Device Classification Name

catheter, percutaneous

510(k) Number K023402
Device Name 8F LAUNCHER GUIDE CATHETER
Original Applicant
MEDTRONIC VASCULAR
37a cherry hill dr.
danvers, 
MA 
01923

Original Contact fred l boucher
Regulation Number 870.1250
Classification Product Code
DQY  
Date Received 10/10/2002
Decision Date 11/06/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls