FDA 510(k) Application Details - K003222

Device Classification Name	Laryngoscope, Endoscope   More FDA Info for this Device
510(K) Number	K003222
Device Name	Laryngoscope, Endoscope
Applicant	COMPUTER MOTION, INC. 130 CREMONA DR., SUITE B GOLETA, CA 93117 US Other 510(k) Applications for this Company
Contact	DAVID U THOMAS 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	10/16/2000
Decision Date	11/03/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review