Class Class II

Tenderfoot (K223352)

K223352 2023-03-02 Special
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Description

Tenderfoot by Accriva Diagnostics, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223352
Clearance Date2023-03-02
Clearance TypeSpecial
Product CodeFMK
Regulation Number878.4850

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