FDA 510(k) Application Details - K974250

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K974250
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	PILLING WECK, INC. 420 DELAWARE DR. FORT WASHINGTON, PA 19034 US Other 510(k) Applications for this Company
Contact	RICHARD G JONES Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/1997
Decision Date	02/11/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review