510(k) K230602 · CAF Nebulizer (Direct Patient Interface)
Hudson RCI® TurboMist Nebulizer System
| Applicant | Medline Industries, LP, Northfiled IL, US |
| Decision | Substantially Equivalent, Oct 31, 2023 |
| Received | Mar 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230602
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.