510(k) K210137 ยท EOX Esophagoscope (Flexible Or Rigid)
EsoCheck Cell Collection Device
| Applicant | Lucid Diagnostics, Inc., New York NY, US |
| Decision | Unknown, Feb 18, 2021 |
| Received | Jan 19, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210137
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.