510(k) K203626 ยท MQK Labware, Assisted Reproduction
SureStrip Vitrification Straw, SureLock Vitrification Straw
| Applicant | Allwin Medical Devices, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Jun 4, 2021 |
| Received | Dec 11, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203626
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.