ATLAS MONITOR, MODELS 200,210,220


Device Classification Name

oximeter

510(k) Number K022084
Device Name ATLAS MONITOR, MODELS 200,210,220
Original Applicant
WELCH ALLYN, INC.
4341 state st. rd.
p.o. box 220
skaneateles falls, 
NY 
13153 -0220

Original Contact shawn earle
Regulation Number 870.2700
Classification Product Code
DQA  
Date Received 06/27/2002
Decision Date 09/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No