510(k) K971303 ยท HHE Cup, Menstrual
INSTEAD, SOFTCUP
| Applicant | Ultrafem, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 6, 1997 |
| Received | Apr 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971303
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.