Keeler, Ltd.

Keeler, Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2010, most recent 2014.

Top product codes for Keeler, Ltd.

Recent clearances by Keeler, Ltd.

K142179 — D-KAT Z-YPECode HKY·2014-09-17
K131787 — CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBESCode HRN·2013-12-23
K131589 — KEELER SLIT LAMP H-SERIESCode HJO·2013-06-27
K093445 — KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT)Code HKY·2010-01-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.