510(k) K770791 ยท KCX Epilator, High Frequency, Tweezer-Type
DEPILATOR, DERMA-I & DERMA-II
| Applicant | Electro-Kinetic Eng/Mfg, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1981 |
| Received | May 2, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770791
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.