510(k) K232836 ยท CBK Ventilator, Continuous, Facility Use
Family of DIMAR DMAX NIV masks
| Applicant | Dimar S.P.A., Medolla, IT |
| Decision | Substantially Equivalent, Aug 14, 2024 |
| Received | Sep 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232836
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.