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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name oximeter, ear
510(k) Number K942752
Device Name MARQUETTE EAR PROBE SENSOR
Applicant
MARQUETTE ELECTRONICS, INC.
100 MARQUETTE DR.
JUPITER,  FL  33468
Applicant Contact MICHAEL LAUGHRAN
Correspondent
MARQUETTE ELECTRONICS, INC.
100 MARQUETTE DR.
JUPITER,  FL  33468
Correspondent Contact MICHAEL LAUGHRAN
Regulation Number870.2710
Classification Product Code
DPZ  
Date Received06/10/1994
Decision Date 09/02/1994
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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