FDA 510(k) Application Details - K962312

Device Classification Name	Needle, Emergency Airway   More FDA Info for this Device
510(K) Number	K962312
Device Name	Needle, Emergency Airway
Applicant	FFRENCH POCKET EMERGENCY AIRWAY, INC. 1705 CALHOUN ST. NEW ORLEANS, LA 70118 US Other 510(k) Applications for this Company
Contact	H. CLAY WILSON, P.E. Other 510(k) Applications for this Contact
Regulation Number	868.5090   More FDA Info for this Regulation Number
Classification Product Code	BWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/1996
Decision Date	06/17/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review