510(k) K973773 ยท KCX Epilator, High Frequency, Tweezer-Type
DAPELLE HAIR REMOVER
| Applicant | Wellquest Intl., Inc., New York NY, US |
| Decision | Substantially Equivalent, Dec 17, 1997 |
| Received | Oct 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973773
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.