510(k) K240605 · MQL Media, Reproductive
Ultra RapidWarm Blast
| Applicant | Vitrolife Sweden AB, Västra Frölunda, SE |
| Decision | Substantially Equivalent, Aug 7, 2024 |
| Received | Mar 4, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240605
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.