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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Airway, Oropharyngeal, Anesthesiology
510(k) Number K854029
Device Name RESPIRATORY RESUSCITATION DEVICE
Applicant
JOHN H. HARRISON
4676 LONG BEACH BLVD. #115
LONG BEACH,  CA  90805
Applicant Contact JOHN H HARRISON
Correspondent
JOHN H. HARRISON
4676 LONG BEACH BLVD. #115
LONG BEACH,  CA  90805
Correspondent Contact JOHN H HARRISON
Regulation Number868.5110
Classification Product Code
CAE  
Date Received10/01/1985
Decision Date 03/11/1986
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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