ACUSTIM


Device Classification Name

stimulator, electro-acupuncture

510(k) Number K014273
Device Name ACUSTIM
Original Applicant
S.H.P. INTL. PTY., LTD.
5/212 glen osmond rd.
fullarton, s.a., 

AU

5063

Original Contact e.d. richards
Classification Product Code
BWK  
Date Received 12/27/2001
Decision Date 06/12/2002
Decision

substantially equivalent

(SESE)

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No