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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name ventilator, emergency, manual (resuscitator)
510(k) Number K904346
Device Name BAUMAN CPR/RESUSCITATOR
Applicant
GENERAL MEDICAL PRODUCTS, INC.
2210 WILSHIRE BLVD, #705
SANTA MONICA,  CA  90403
Applicant Contact JACK BAUMAN
Correspondent
GENERAL MEDICAL PRODUCTS, INC.
2210 WILSHIRE BLVD, #705
SANTA MONICA,  CA  90403
Correspondent Contact JACK BAUMAN
Regulation Number868.5915
Classification Product Code
BTM  
Date Received09/24/1990
Decision Date 10/02/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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