FDA 510(k) Applications Submitted by KEELER LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K142179 08/08/2014 D-KAT Z-YPE KEELER LTD.
K131787 06/18/2013 CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBES KEELER LTD.
K093445 10/21/2009 KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT) KEELER LTD.
K131589 05/31/2013 KEELER SLIT LAMP H-SERIES KEELER LTD.


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