Class Class II

The Alma Soprano Titanium (K230371)

K230371 2023-02-22 Special
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Description

The Alma Soprano Titanium by Alma Lasers, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230371
Clearance Date2023-02-22
Clearance TypeSpecial
Product CodeGEX
Regulation Number878.4810

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