Class Class II

Renuvion® APR Handpiece (K230272)

K230272 2023-04-27 Traditional
Home/ Devices/ Renuvion® APR Handpiece (K230272)

Description

Renuvion® APR Handpiece by Apyx Medical Corporation — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230272
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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