510(k) K162051 ยท MQK Labware, Assisted Reproduction
Cryotec
| Applicant | Reprolife, Inc., Shinjuku-Ku, JP |
| Decision | Substantially Equivalent, Dec 14, 2016 |
| Received | Jul 25, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162051
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.