510(k) K210126 ยท CAF Nebulizer (Direct Patient Interface)
Sodium Chloride Inhalation Solutions, 3%, 3.5%, 7% and 10%
| Applicant | The Ritedose Corporation, Columbia SC, US |
| Decision | Substantially Equivalent, Dec 3, 2021 |
| Received | Jan 19, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210126
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.