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The Lebanon Corp.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K841652 OCULAR PRESSURE APPLICATOR1984-06-01 View
510(k) K821689 LEBANON MICROSCOPEEPT1982-07-09 View
510(k) K820526 RELIEF VALVE-HONAN INTRAOC. PRESSURELCC1982-03-25 View
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