MICROPAQ, MODELS 402, 404


Device Classification Name

monitor, cardiac (incl. cardiotachometer & rate alarm)

510(k) Number K021681
Device Name MICROPAQ, MODELS 402, 404
Original Applicant
WELCH ALLYN PROTOCOL, INC.
8500 s.w. creekside place
beaverton, 
OR 
97008 -7107

Original Contact don m abbey
Regulation Number 870.2300
Classification Product Code
DRT  
Subsequent Product Code
DQA  
Date Received 05/22/2002
Decision Date 07/23/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No