KARMA 800 SERIES MANUAL WHEELCHAIR


Device Classification Name

wheelchair, mechanical

510(k) Number K021866
Device Name KARMA 800 SERIES MANUAL WHEELCHAIR
Original Applicant
VESTIL MANUFACTURING CORP.
900 growth pkwy.
angola, 
IN 
46703

Original Contact rick michael
Regulation Number 890.3850
Classification Product Code
IOR  
Date Received 06/06/2002
Decision Date 06/14/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Physical Medicine

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No