FDA 510(k) Application Details - K984240

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K984240
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	ETHICON ENDO-SURGERY, INC. 4545 CREEK RD. CINCINNATI, OH 45242-2839 US Other 510(k) Applications for this Company
Contact	JACKIE A STRASSER 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	11/27/1998
Decision Date	06/22/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review