510(k) K213835 ยท NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
TENS & EMS Device
| Applicant | Shenzhen Jian Feng Electronic Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Mar 3, 2022 |
| Received | Dec 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213835
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.