510(k) K991264 ยท MQE Needle, Assisted Reproduction
<GENX> SINGLE LUMEN SIDEPORT NEEDLE
| Applicant | <Genx> Intl., Inc., Madison CT, US |
| Decision | Substantially Equivalent, Sep 9, 1999 |
| Received | Apr 13, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991264
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.