510(k) K080040 ยท HDW Diaphragm, Contraceptive (And Accessories)
ORTHO ALL-FLEX DIAPHRAGM
| Applicant | Johnson & Johnson Produtos Profissionais Ltda., Claremont NH, US |
| Decision | Substantially Equivalent, Aug 25, 2008 |
| Received | Jan 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080040
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.