FDA 510(k) Application Details - K150024

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K150024
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	GUENTER BISSINGER MEDIZINTECHNIK GMBH HANS-THEISEN-STR. 1 TENINGEN 79331 DE Other 510(k) Applications for this Company
Contact	Matthias Bissinger 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	01/07/2015
Decision Date	02/20/2015
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