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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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