AUTOPULSE RESUSCITATION SYSTEM


Device Classification Name

compressor, cardiac, external

510(k) Number K022345
Device Name AUTOPULSE RESUSCITATION SYSTEM
Original Applicant
REVIVANT CORP.
775 palomar ave.
sunnyvale, 
CA 
94085

Original Contact susanne t smith
Regulation Number 870.5200
Classification Product Code
DRM  
Date Received 07/19/2002
Decision Date 08/15/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls