510(k) K170205 ยท NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203
| Applicant | Shenzhen Kentro Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, May 11, 2017 |
| Received | Jan 23, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170205
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.