Class Class II

Verifine® Ease Lancing Device, Verifine® Lancing Device (K223643)

K223643 2023-02-21 Traditional
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Description

Verifine® Ease Lancing Device, Verifine® Lancing Device by Promisemed Hangzhou Meditech Co., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223643
Clearance Date2023-02-21
Clearance TypeTraditional
Product CodeQRL
Regulation Number878.4850

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