Class Class II

AviClear Laser System (K230660)

K230660 2023-06-06 Traditional
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Description

AviClear Laser System by Cutera, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230660
Clearance Date2023-06-06
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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