Class Class II

Epildream HP 4000 MED (K222352)

K222352 2023-04-27 Traditional
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Description

Epildream HP 4000 MED by D.E.A Project S.R.1. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222352
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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