510(k) K200815 · MQK Labware, Assisted Reproduction
VitriGuard
| Applicant | Origio A/S, Måløv, DK |
| Decision | Substantially Equivalent, Jun 25, 2020 |
| Received | Mar 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200815
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.