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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Emergency Airway
510(k) Number K962312
Device Name KEY CHAIN EMERGENCY AIRWAY
Applicant
FFRENCH POCKET EMERGENCY AIRWAY, INC.
1705 CALHOUN ST.
NEW ORLEANS,  LA  70118
Applicant Contact H. CLAY WILSON, P.E.
Correspondent
FFRENCH POCKET EMERGENCY AIRWAY, INC.
1705 CALHOUN ST.
NEW ORLEANS,  LA  70118
Correspondent Contact H. CLAY WILSON, P.E.
Regulation Number868.5090
Classification Product Code
BWC  
Date Received06/17/1996
Decision Date 06/17/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
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