FDA 510(k) Application Details - K960400

Device Classification Name	Cannula And Trocar, Suprapubic, Non-Disposable   More FDA Info for this Device
510(K) Number	K960400
Device Name	Cannula And Trocar, Suprapubic, Non-Disposable
Applicant	SNOWDEN-PENCER 5175 SOUTH ROYAL ATLANTA DR. TUCKER, GA 30084 US Other 510(k) Applications for this Company
Contact	JULIE A STEPHENS Other 510(k) Applications for this Contact
Regulation Number	876.5090   More FDA Info for this Regulation Number
Classification Product Code	FBM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/1996
Decision Date	03/12/1996
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