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Aesculap-Meditec GmbH

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K991993 PHACOLASE ER: YAG LASERGEX1999-11-17 View
510(k) K983215 MULTIPULSE CO2 LASERGEX1998-12-04 View
510(k) K964128 MCL 29 DERMABLATE ERBIUM LASER SYSTEMGEX1997-03-17 View
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