THUMPER, MODEL: 1008


Device Classification Name

compressor, cardiac, external

510(k) Number K073079
Device Name THUMPER, MODEL: 1008
Applicant
MICHIGAN INSTRUMENTS, INC.
555 thirteenth st., nw
washington, 
DC 
20004

Applicant Contact howard m hostein
Correspondent
MICHIGAN INSTRUMENTS, INC.
555 thirteenth st., nw
washington, 
DC 
20004

Correspodent Contact howard m hostein
Regulation Number 870.5200
Classification Product Code
DRM  
Date Received 10/31/2007
Decision Date 02/14/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No