KOKOMATE


Device Classification Name

spirometer, diagnostic

510(k) Number K022276
Device Name KOKOMATE
Original Applicant
FERRARIS RESPIRATORY, INC.
908 main st.
louisville, 
CO 
80027

Original Contact jim lewis
Regulation Number 868.1840
Classification Product Code
BZG  
Date Received 07/15/2002
Decision Date 10/04/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No