Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494)— 510(k) K242332
Substantially EquivalentShenzhen Kentro Medical Electronics Co., Ltd.
FDA 510(k) clearance K242332 for Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494), Substantially Equivalent on 2024-11-05. Applicant: Shenzhen Kentro Medical Electronics Co., Ltd..
Clearance details
- Applicant
- Shenzhen Kentro Medical Electronics Co., Ltd.
- Product code
- Code NUH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.