FDA 510(k) Application Details - K993885

Device Classification Name	Electrode, Electrosurgical   More FDA Info for this Device
510(K) Number	K993885
Device Name	Electrode, Electrosurgical
Applicant	LINVATEC CORP. 11311 CONCEPT BLVD. LARGO, FL 33773-4908 US Other 510(k) Applications for this Company
Contact	LAURA SENEFF Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	JOS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/16/1999
Decision Date	02/10/2000
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