510(k) K261829 · FMI Needle, Hypodermic, Single Lumen
Profoject Dual-Safety Pen Needles
| Applicant | CMT Health PTE., Ltd., Singapore, SG |
| Decision | Substantially Equivalent, Jul 29, 2026 |
| Received | Jun 2, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261829
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.