Class Class II

Claritag Advanced (K222356)

K222356 2023-05-18 Traditional
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Description

Claritag Advanced by Dgi Technologies — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222356
Clearance Date2023-05-18
Clearance TypeTraditional
Product CodeGEH
Regulation Number878.4350

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