FDA 510(k) Application Details - K962387

Device Classification Name	Dislodger, Stone, Basket, Ureteral, Metal   More FDA Info for this Device
510(K) Number	K962387
Device Name	Dislodger, Stone, Basket, Ureteral, Metal
Applicant	OLYMPUS AMERICA, INC. TWO CORPORATE CENTER DR. MELVILLE, NY 11747-3157 US Other 510(k) Applications for this Company
Contact	BARRY E SANDS Other 510(k) Applications for this Contact
Regulation Number	876.4680   More FDA Info for this Regulation Number
Classification Product Code	FFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/1996
Decision Date	07/31/1996
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