MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM


Device Classification Name

detector and alarm, arrhythmia

510(k) Number K022453
Device Name MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM
Original Applicant
WELCH ALLYN PROTOCOL, INC.
8500 s.w. creekside place
beaverton, 
OR 
97008 -7107

Original Contact don m abbey
Regulation Number 870.1025
Classification Product Code
DSI  
Date Received 07/26/2002
Decision Date 08/21/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls