FDA 510(k) Application Details - K955501

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K955501
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	THE TULIP MFG. CO. 40 WEST BASELINE RD., SUITE 120 MESA, AZ 85210 US Other 510(k) Applications for this Company
Contact	RICHARD S HUNTER 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	12/01/1995
Decision Date	01/17/1996
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