FDA 510(k) Application Details - K101049

Device Classification Name	Unit, Cryosurgical, Accessories   More FDA Info for this Device
510(K) Number	K101049
Device Name	Unit, Cryosurgical, Accessories
Applicant	KONINKLIJKE UTERMOHLEN NV 4 INNOVATION DRIVE DUNDAS, ONTARIO L9H 7P3 CA Other 510(k) Applications for this Company
Contact	SHIRLEY FURESZ Other 510(k) Applications for this Contact
Regulation Number	878.4350   More FDA Info for this Regulation Number
Classification Product Code	GEH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/14/2010
Decision Date	06/23/2011
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