510(k) K161484 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
ZIIP Device
| Applicant | Ziip,Llc, Piedmont CA, US |
| Decision | Substantially Equivalent, Feb 24, 2017 |
| Received | May 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161484
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.