510(k) K210399 ยท FMI Needle, Hypodermic, Single Lumen
Unifine SafeControl
| Applicant | Owen Mumford, Ltd., Woodstock, GB |
| Decision | Substantially Equivalent, Sep 17, 2021 |
| Received | Feb 10, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210399
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.