Class Class II

Myolift QT (K213078)

K213078 2023-04-27 Traditional
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Description

Myolift QT by Johari Digital Healthcare Limited — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213078
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodeNFO
Regulation Number882.5890

Categories

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