Class Class II

Plasma IQ (K223222)

K223222 2023-01-17 Special
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Description

Plasma IQ by Neauvia North America, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223222
Clearance Date2023-01-17
Clearance TypeSpecial
Product CodeGEI
Regulation Number878.4400

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