510(k) K952117 ยท KCX Epilator, High Frequency, Tweezer-Type
EPILATOR
| Applicant | Burke Neutech, Inc., St. Petersburg FL, US |
| Decision | Substantially Equivalent, Oct 19, 1995 |
| Received | May 5, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952117
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.