510(k) K101333

CRYOCARE CS SURGICAL SYSTEM by Endocare, Inc. — Product Code GEH

K101333 is an FDA 510(k) premarket notification submitted by Endocare, Inc. for the device "CRYOCARE CS SURGICAL SYSTEM". The FDA issued a decision of Substantially Equivalent on June 14, 2010. The device falls under product code GEH (Unit, Cryosurgical, Accessories), a Class II device regulated under 21 CFR 878.4350. Endocare, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 2010
Date Received
May 12, 2010
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Unit, Cryosurgical, Accessories
Device Class
Class II
Regulation Number
878.4350
Review Panel
SU
Submission Type