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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 K872626
Device Name OXIMETRY MODULE
Applicant
MARQUETTE ELECTRONICS, INC.
8200 WEST TOWER AVE.
MILWAUKEE,  WI  53223
Applicant Contact THOMAS MASSOPUST
Correspondent
MARQUETTE ELECTRONICS, INC.
8200 WEST TOWER AVE.
MILWAUKEE,  WI  53223
Correspondent Contact THOMAS MASSOPUST
Regulation Number870.2700
Classification Product Code
DQA  
Date Received07/06/1987
Decision Date 09/15/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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