510(k) K140207 ยท MQK Labware, Assisted Reproduction
RAPID-I KIT
| Applicant | Vitrolife Sweden AB, Washington DC, US |
| Decision | Substantially Equivalent, Dec 18, 2014 |
| Received | Jan 28, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140207
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.