FDA 510(k) Application Details - K021747

Device Classification Name	Laryngoscope, Endoscope   More FDA Info for this Device
510(K) Number	K021747
Device Name	Laryngoscope, Endoscope
Applicant	SURGICON, INC. 400 LONG BEACH BLVD. STRATFORD, CT 06615 US Other 510(k) Applications for this Company
Contact	CURTIS RAYMOND Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	GCI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/28/2002
Decision Date	08/15/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review