Cranial Electrical Nerve Stimulator, Model Fm 10/C

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K090052 ↗

FDA Product Code

QJQ

FDA applicant

Johari Digital Healthcare , Ltd.

Device Class

Class II

Regulation

21 CFR Part 882.5800

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

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