ENVOY


Device Classification Name

oximeter

510(k) Number K022168
Device Name ENVOY
Original Applicant
MENNEN MEDICAL LTD.
10123 main st.
clarence, 
NY 
14031

Original Contact david p johnson
Regulation Number 870.2700
Classification Product Code
DQA  
Subsequent Product Code
DSI  
Date Received 07/03/2002
Decision Date 08/01/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No