510(k) K873388

KEELER CTU CRYO SYSTEM by Keeler Instruments, Inc. — Product Code HPS

K873388 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "KEELER CTU CRYO SYSTEM". The FDA issued a decision of Substantially Equivalent on November 13, 1987. The device falls under product code HPS (Unit, Cryophthalmic), 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 13, 1987
Date Received
August 24, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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