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Kera Corp.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K901009 MODEL 2000 INTRAOPERATIVE CORNEASCOPEHLQ1990-05-30 View
510(k) K871479 VIDEOSCAN (TM)HLQ1987-05-22 View
510(k) K864037 KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZERHJB1986-11-13 View
510(k) K850665 CORNEASCOPE MODEL 1200HLQ1985-03-20 View
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