FDA 510(k) Application Details - K001408

Device Classification Name	Angioscope   More FDA Info for this Device
510(K) Number	K001408
Device Name	Angioscope
Applicant	KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE CULVER CITY, CA 90230-7600 US Other 510(k) Applications for this Company
Contact	KEVIN KENNAN Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	LYK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/04/2000
Decision Date	10/30/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review