FDA 510(k) Application Details - K993306

Device Classification Name	Apparatus, Electrosurgical   More FDA Info for this Device
510(K) Number	K993306
Device Name	Apparatus, Electrosurgical
Applicant	PALADIN MEDICAL, INC. P.O. BOX 560 STILLWATER, MN 55082-0560 US Other 510(k) Applications for this Company
Contact	ELAINE DUNCAN, M.S.M.E., RAC Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	HAM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/04/1999
Decision Date	11/03/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review