510(k) K252518 ยท FMF Syringe, Piston
DuoprossTM Smart Cap (Type I)
| Applicant | Duopross Meditech Corporate, Farmingdale NY, US |
| Decision | Substantially Equivalent, Dec 17, 2025 |
| Received | Aug 11, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252518
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.