Class Class II

SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories (K221306)

K221306 2023-01-27 Traditional
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Description

SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories by Gyrus Acmi, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221306
Clearance Date2023-01-27
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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