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Gentex Corporation

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080117 PATIENT ISOLATION UNIT, MODEL G019-1000LGM2009-01-30 View
510(k) K800521 THE LENS OR OMMI-GARDHQG1980-03-12 View
510(k) K772024 RX LENS SERIESHQG1977-11-09 View
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