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Optical Diagnostic Device For Melanoma Detection

FDA product code OYD · Class 2 · General, Plastic Surgery

0
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2015-04-02MELA Sciences, Inc.The probability and histogram data within the Melafind's device displayed user interface lacks approval (not included in the PMA supplement).

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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