510(k) K202340 ยท FMI Needle, Hypodermic, Single Lumen
Droplet Pen Needle 30G & 33G
| Applicant | Htl-Strefa S.A, Ozorkow, PL |
| Decision | Substantially Equivalent, Oct 15, 2020 |
| Received | Aug 17, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202340
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.