LIVESIRE ELECTROPHYSIOLOGY CATHETER


Device Classification Name

catheter, electrode recording, or probe, electrode recording

510(k) Number K022380
Device Name LIVESIRE ELECTROPHYSIOLOGY CATHETER
Original Applicant
ST. JUDE MEDICAL
14900 minnetonka industrial bl
minnetonka, 
MN 
55345

Original Contact jim m taufen
Regulation Number 870.1220
Classification Product Code
DRF  
Date Received 07/22/2002
Decision Date 10/01/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No