FDA 510(k) Application Details - K955261

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K955261
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	MSB LTD. HILLDROP LANE, RAMSBURY MARLBOROUGH, WILTSHIRE SN8 2RB GB Other 510(k) Applications for this Company
Contact	HELEN BARNES 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	11/09/1995
Decision Date	01/30/1996
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