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Laser Center Dev. Corp.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K981235 OCULOSTATHNC1998-07-15 View
510(k) K981063 AUTOMATED CORNEAL TREPHINEHRG1998-06-23 View
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