510(k) K192008 ยท MRX System, Assisted Reproduction Laser
LaserShot M, NaviLase
| Applicant | Vitrolife GmbH, Bruckberg, DE |
| Decision | Substantially Equivalent, Mar 25, 2020 |
| Received | Jul 29, 2019 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K192008
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.