510(k) K062412

CRYOMATIC by Keeler Instruments, Inc. — Product Code HRN

K062412 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "CRYOMATIC". The FDA issued a decision of Substantially Equivalent on November 6, 2006. The device falls under product code HRN (Unit, Cryophthalmic, Ac-Powered), a Class II device regulated under 21 CFR 886.4170. Keeler Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 2006
Date Received
August 17, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Cryophthalmic, Ac-Powered
Device Class
Class II
Regulation Number
886.4170
Review Panel
OP
Submission Type