FDA 510(k) Application Details - K041783

Device Classification Name	Unit, Cryosurgical, Accessories   More FDA Info for this Device
510(K) Number	K041783
Device Name	Unit, Cryosurgical, Accessories
Applicant	CHEK-MED SYSTEMS 25 VILLAGE HILL RD. WILLINGTON, CT 06279 US Other 510(k) Applications for this Company
Contact	ROB WHALEN 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	07/01/2004
Decision Date	09/28/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review