FDA 510(k) Application Details - K021731

Device Classification Name	Laparoscope, General & Plastic Surgery   More FDA Info for this Device
510(K) Number	K021731
Device Name	Laparoscope, General & Plastic Surgery
Applicant	TAUT, INC. 2571 KANEVILLE COURT GENEVA, IL 60134 US Other 510(k) Applications for this Company
Contact	MAX CLOAT Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	GCJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/24/2002
Decision Date	08/08/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review