510(k) K173075 · MQK Labware, Assisted Reproduction
ZyMot ICSI Sperm Separation Device, ZyMot Multi Sperm Separation Device (850µl, 3ml)
| Applicant | Dxnow, Inc., Gaithersburg MD, US |
| Decision | Substantially Equivalent, Mar 8, 2018 |
| Received | Sep 29, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K173075
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.