510(k) K212342 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
ZIIP+ Device
| Applicant | Ziip, Inc., Oakland CA, US |
| Decision | Substantially Equivalent, Sep 23, 2021 |
| Received | Jul 28, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212342
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.