PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM


Device Classification Name

spirometer, diagnostic

510(k) Number K022103
Device Name PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM
Original Applicant
PURITAN BENNETT CORP.
2200 faraday ave.
carlsbad, 
CA 
92008

Original Contact james bonds
Regulation Number 868.1840
Classification Product Code
BZG  
Date Received 06/28/2002
Decision Date 09/27/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No