Class Class II

PALLAS Premium (K223588)

K223588 2023-01-26 Traditional
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Description

PALLAS Premium by Laseroptek Co., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223588
Clearance Date2023-01-26
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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