FDA 510(k) Application Details - K960574

Device Classification Name	Pneumoperitoneum Needle   More FDA Info for this Device
510(K) Number	K960574
Device Name	Pneumoperitoneum Needle
Applicant	SHERWOOD MEDICAL CO. 1915 OLIVE ST. ST. LOUIS, MO 63103-1642 US Other 510(k) Applications for this Company
Contact	DENNIS POZZO Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FHO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/12/1996
Decision Date	08/05/1996
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