EMS/TENS Massager Device— 510(k) K233040

Substantially Equivalent

Shenzhen Imdk Medical Technology Co., Ltd.

FDA 510(k) clearance K233040 for EMS/TENS Massager Device, Substantially Equivalent on 2024-02-12. Applicant: Shenzhen Imdk Medical Technology Co., Ltd..

Clearance details

Applicant: Shenzhen Imdk Medical Technology Co., Ltd.
Product code: Code NUH
Advisory panel: Neurology
Date received: 2023-09-25
Decision date: 2024-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

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