FDA 510(k) Application Details - K954171

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K954171
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	HOLL MEDITRONICS, INC. 4 MARCONI COURT BOLTON, ONTARIO L7E 1E7 CA Other 510(k) Applications for this Company
Contact	WILLIAM H HOLL 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	09/05/1995
Decision Date	04/30/1996
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