510(k) K173881 ยท FMI Needle, Hypodermic, Single Lumen
Unifine SafeControl 5mm x 30G, Unifine SafeControl 8mm x 30G
| Applicant | Owen Mumford, Ltd., Woodstock, GB |
| Decision | Substantially Equivalent, Jul 11, 2018 |
| Received | Dec 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173881
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.