Low-Frequency Multi-function Physiotherapy Instrument (Model: KTR-2230, KTR-2220, KTR-2210, KTR-2231, KTR-2221, KTR-2211, KTR-2232, KTR-2222, KTR-2212)— 510(k) K191982
Substantially EquivalentShenzhen Kentro Medical Electronics Co., Ltd.
FDA 510(k) clearance K191982 for Low-Frequency Multi-function Physiotherapy Instrument (Model: KTR-2230, KTR-2220, KTR-2210, KTR-2231, KTR-2221, KTR-2211, KTR-2232, KTR-2222, KTR-2212), Substantially Equivalent on 2020-09-25. Applicant: Shenzhen Kentro Medical Electronics Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Kentro Medical Electronics Co., Ltd.
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen City, CN
Recent devices under product code NUH
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