FDA 510(k) Application Details - K974593

Device Classification Name	Forceps   More FDA Info for this Device
510(K) Number	K974593
Device Name	Forceps
Applicant	TITAN MFG., INC. 6 JAMIE LN. PHOENIXVILLE, PA 19460 US Other 510(k) Applications for this Company
Contact	DONALD SEAVEY Other 510(k) Applications for this Contact
Regulation Number	878.4800   More FDA Info for this Regulation Number
Classification Product Code	HTD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/09/1997
Decision Date	06/24/1998
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