510(k) K162640 ยท MQK Labware, Assisted Reproduction
iVitri EZ
| Applicant | Reprobitech Corp., New Hyde Park NY, US |
| Decision | Substantially Equivalent, Jun 30, 2017 |
| Received | Sep 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162640
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.