510(k) K191982 ยท NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
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)
| Applicant | Shenzhen Kentro Medical Electronics Co., Ltd., Shenzhen City, CN |
| Decision | Substantially Equivalent, Sep 25, 2020 |
| Received | Jul 25, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191982
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.