CEFAR REHAB 2 AND REHAB 2 PRO


Device Classification Name

stimulator, muscle, powered

510(k) Number K030403
Device Name CEFAR REHAB 2 AND REHAB 2 PRO
Applicant
CEFAR MEDICAL AB
6740 riverview terrace
minneapolis, 
MN 
55432

Applicant Contact constance g bundy
Correspondent
CEFAR MEDICAL AB
6740 riverview terrace
minneapolis, 
MN 
55432

Correspodent Contact constance g bundy
Regulation Number 890.5850
Classification Product Code
IPF  
Date Received 02/06/2003
Decision Date 07/17/2003
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