510(k) K203792 ยท FMI Needle, Hypodermic, Single Lumen
Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle
| Applicant | Pikdare Spa, Casnate Con Bernate, IT |
| Decision | Substantially Equivalent, Jan 20, 2023 |
| Received | Dec 28, 2020 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K203792
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.