510(k) K172050 · MQE Needle, Assisted Reproduction
Follicle Aspiration Set, Reduced Single Lumen
| Applicant | Vitrolife Sweden AB, Västra Frölunda, SE |
| Decision | Substantially Equivalent, Nov 21, 2017 |
| Received | Jul 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172050
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.