FDA 510(k) Application Details - K063368

Device Classification Name	Needle, Fistula   More FDA Info for this Device
510(K) Number	K063368
Device Name	Needle, Fistula
Applicant	NIPRO MEDICAL CORP. 3150 NW 107 AVE.. MIAMI, FL 33172 US Other 510(k) Applications for this Company
Contact	JESSICA OSWALD Other 510(k) Applications for this Contact
Regulation Number	876.5540   More FDA Info for this Regulation Number
Classification Product Code	FIE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/07/2006
Decision Date	02/05/2007
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