510(k) K091754 ยท HHE Cup, Menstrual
LUNETTE MENSTRUAL CUP, MODELS 1 AND 2
| Applicant | Lune Group , Ltd., Madison WI, US |
| Decision | Substantially Equivalent, Nov 13, 2009 |
| Received | Jun 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091754
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.