510(k) K973340 ยท KCX Epilator, High Frequency, Tweezer-Type
TWEEZER-TYPE EPILATOR
| Applicant | Mobit, Inc., New York NY, US |
| Decision | Substantially Equivalent, Dec 3, 1997 |
| Received | Sep 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973340
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.