Class Class II

DeepX DermoSight Dermatoscope (K230448)

K230448 2023-05-17 Traditional
Home/ Devices/ DeepX DermoSight Dermatoscope (K230448)

Description

DeepX DermoSight Dermatoscope by Deepx Health, LLC — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230448
Clearance Date2023-05-17
Clearance TypeTraditional
Product CodePSN
Regulation Number878.4580

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