510(k) K133295 ยท MQK Labware, Assisted Reproduction
QUALIS
| Applicant | Menicon Co., Ltd. New Business Division, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 18, 2014 |
| Received | Oct 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133295
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.