FDA 510(k) Application Details - K992904

Device Classification Name	Catheter, Peritoneal   More FDA Info for this Device
510(K) Number	K992904
Device Name	Catheter, Peritoneal
Applicant	TAUT, INC. 2571 KANEVILLE COURT GENEVA, IL 60134 US Other 510(k) Applications for this Company
Contact	RONALD KENSETH Other 510(k) Applications for this Contact
Regulation Number	878.4200   More FDA Info for this Regulation Number
Classification Product Code	GBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/1999
Decision Date	10/05/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review