Class Class II

Tens & Ems Device (K223825)

K223825 2023-05-09 Traditional
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Description

Tens & Ems Device by Shenzhen Jian Feng Electronic Technology Co., Ltd. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223825
Clearance Date2023-05-09
Clearance TypeTraditional
Product CodeNUH
Regulation Number882.5890

Categories

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