FDA 510(k) Application Details - K100258

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K100258
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	WICKIMED SUPPLY LIMITED RM25, 11/F. 19 SHING YIP ST. KWUN TONG, KLN HONG KONG CN Other 510(k) Applications for this Company
Contact	KIPSON FUNG 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	01/28/2010
Decision Date	04/28/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review