510(k) K241248 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Quantum Perfusion Dual Lumen Cannula 31F-V1 (DL31F-V1)
| Applicant | Spectrum Medical S.R.L., Mirandola, IT |
| Decision | Substantially Equivalent, May 31, 2024 |
| Received | May 3, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241248
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.