FDA 510(k) Application Details - K954787

Device Classification Name	Laryngoscope, Rigid   More FDA Info for this Device
510(K) Number	K954787
Device Name	Laryngoscope, Rigid
Applicant	HOSPITAK, INC. 10 DANIEL ST. FARMINGDALE, NY 11735 US Other 510(k) Applications for this Company
Contact	WILLIAM LACCY Other 510(k) Applications for this Contact
Regulation Number	868.5540   More FDA Info for this Regulation Number
Classification Product Code	CCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/18/1995
Decision Date	01/31/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review