510(k) K970338 ยท KCX Epilator, High Frequency, Tweezer-Type
TWEEZER-TYPE EPILATOR
| Applicant | Igia Direct, Inc., Westford MA, US |
| Decision | Substantially Equivalent, Jul 1, 1997 |
| Received | Jan 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970338
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.