510(k) K241341 ยท MQK Labware, Assisted Reproduction
cryo-GO Vitrification Device
| Applicant | Fujifilm Irvine Scientific, Santa Ana CA, US |
| Decision | Substantially Equivalent, Sep 26, 2024 |
| Received | May 13, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241341
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.