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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 K890033
Device Name MODEL 8700 PULSE OXIMETER
Original Applicant
NONIN MEDICAL, INC.
12900 highway 55
minneapolis,  MN  55441
Original Contact neal f nordling
Regulation Number870.2700
Classification Product Code
DQA  
Date Received01/04/1989
Decision Date 02/06/1989
Decision substantially equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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