FDA 510(k) Application Details - K152203

Device Classification Name	Unit, Cryosurgical, Accessories   More FDA Info for this Device
510(K) Number	K152203
Device Name	Unit, Cryosurgical, Accessories
Applicant	KONINKLIJKE (ROYAL) UTERMOHLEN DEE OVERWEG 1 WOLVEGA 8471ZA NL Other 510(k) Applications for this Company
Contact	MR.D VAN HOOF 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	08/06/2015
Decision Date	11/06/2015
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