510(k) K072019 ยท CAF Nebulizer (Direct Patient Interface)
AKITA2 APIXNEB
| Applicant | Activaero America, Inc., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Nov 5, 2007 |
| Received | Jul 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072019
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.