510(k) K260739 · FMI Needle, Hypodermic, Single Lumen
Profoject Pen Needles (Model A; Model B)
| Applicant | CMT Health PTE., Ltd., Singapore, SG |
| Decision | Substantially Equivalent, Jul 15, 2026 |
| Received | Mar 6, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260739
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.