BIOMOVE 5000 SYSTEM


Device Classification Name

stimulator, muscle, powered

510(k) Number K080787
Device Name BIOMOVE 5000 SYSTEM
Applicant
CURATRONIC, LTD.
20 hata ‘ as st.
kfar saba, 

IL

44425

Applicant Contact ahava stein
Correspondent
CURATRONIC, LTD.
20 hata ‘ as st.
kfar saba, 

IL

44425

Correspodent Contact ahava stein
Regulation Number 890.5850
Classification Product Code
IPF  
Date Received 03/20/2008
Decision Date 04/17/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Physical Medicine

510k Review Panel

Neurology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No