510(k) K170835 ยท EGJ Device, Iontophoresis, Other Uses
Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE
| Applicant | Hightech Development, Prague, CZ |
| Decision | Substantially Equivalent, Jun 15, 2018 |
| Received | Mar 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170835
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.