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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name oximeter
510(k) Number K874947
Device Name MODEL 8800 CARDIORESPIRATORY OXIMETER
Original Applicant
NONIN MEDICAL, INC.
13030 highway 55
plymouth,  MA  55441
Original Contact neal f nordling
Regulation Number870.2700
Classification Product Code
DQA  
Date Received12/02/1987
Decision Date 02/12/1988
Decision substantially equivalent (SE)
Classification Advisory Committee Anesthesiology
Review Advisory Committee Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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