510(k) K920792 ยท HHE Cup, Menstrual
SOFTCUP(TM):2
| Applicant | Ultrafem, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 5, 1993 |
| Received | Feb 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920792
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.