510(k) K772322 ยท KCX Epilator, High Frequency, Tweezer-Type
DEPILATORY, ELECTRONIC
| Applicant | Dura Corp., The, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 3, 1978 |
| Received | Dec 19, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772322
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.