510(k) K183262 ยท EOX Esophagoscope (Flexible Or Rigid)
EsoCheck CCD Cell Collection Device
| Applicant | Lucid Diagnostics, Inc., New York NY, US |
| Decision | Unknown, Jun 21, 2019 |
| Received | Nov 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183262
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.