FDA 510(k) Application Details - K020702

Device Classification Name	Anoscope And Accessories   More FDA Info for this Device
510(K) Number	K020702
Device Name	Anoscope And Accessories
Applicant	CANADIAN THEATRE PRODUCTS LTD. #210-828 HARBOUSIDE DR. NORTH VANCOUVER, B.C. V7P 3R9 CA Other 510(k) Applications for this Company
Contact	ANN-MARIE O'KEEFE Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FER Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2002
Decision Date	03/29/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review