FDA 510(k) Application Details - K062918

Device Classification Name	Cystourethroscope   More FDA Info for this Device
510(K) Number	K062918
Device Name	Cystourethroscope
Applicant	KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE 5TH FLOOR CULVER CITY, CA 90230-7600 US Other 510(k) Applications for this Company
Contact	SUSIE CHEN Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FBO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2006
Decision Date	01/17/2007
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