Class Class II

Agnes (K223805)

K223805 2023-05-04 Traditional
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Description

Agnes by Agnes Medical Co., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223805
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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