510(k) K200017 ยท FMI Needle, Hypodermic, Single Lumen
Eclipse DermaFlex Cannula
| Applicant | Eclipse Medcorp, LLC, The Colony TX, US |
| Decision | Substantially Equivalent, Nov 5, 2020 |
| Received | Jan 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200017
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.