FDA 510(k) Application Details - K082565

Device Classification Name	System, Ablation, Microwave And Accessories   More FDA Info for this Device
510(K) Number	K082565
Device Name	System, Ablation, Microwave And Accessories
Applicant	MICROSURGEON, INC. 20363 EAST TULIP CIRCLE MONTROSE, CO 81403 US Other 510(k) Applications for this Company
Contact	DUDLEY HARRIS Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	NEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2008
Decision Date	02/12/2009
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