Class Class II

ATTIVA (K220505)

K220505 2023-02-09 Traditional
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Description

ATTIVA by Italian Engineering S.R.L. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220505
Clearance Date2023-02-09
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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