510(k) K031622 ยท MQE Needle, Assisted Reproduction
WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS
| Applicant | Portex , Ltd., England Ct21 6db, GB |
| Decision | Substantially Equivalent, Jun 26, 2003 |
| Received | May 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031622
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.