510(k) K223353 ยท FMI Needle, Hypodermic, Single Lumen
DropSafeTM SicuraTM
| Applicant | Pikdare Spa, Casnate Con Bernate, IT |
| Decision | Substantially Equivalent, Dec 2, 2022 |
| Received | Nov 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223353
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.