Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Keeler, Ltd.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K131787 CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBESHRN2013-12-23 View
510(k) K131589 KEELER SLIT LAMP H-SERIESHJO2013-06-27 View
510(k) K093445 KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT)HKY2010-01-19 View
↑