510(k) K090832 ยท MQK Labware, Assisted Reproduction
RAPID-I
| Applicant | Vitrolife Sweden AB, Se-400 92 Goteborg, SE |
| Decision | Substantially Equivalent, Dec 23, 2009 |
| Received | Mar 26, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090832
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.