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Sharplight Technologies, Ltd.

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

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K233304 Omnimax S3, Omnimax S4GEX2023-12-22 View
510(k) K173169 Rapid FamilyGEX2017-11-20 View
510(k) K111303 DERMATOLOGICAL TREATMENT DEVICE FAMILYGEX2011-12-21 View
510(k) K082876 BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILYGEX2008-11-10 View
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