FDA 510(k) Application Details - K100520

Device Classification Name	Needle, Fistula   More FDA Info for this Device
510(K) Number	K100520
Device Name	Needle, Fistula
Applicant	NIPRO MEDICAL CORPORATION 3150 N.W. 107TH 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	02/23/2010
Decision Date	03/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review