510(k) K120939 ยท CAF Nebulizer (Direct Patient Interface)
AERONEB PRO
| Applicant | Aerogen, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Apr 26, 2012 |
| Received | Mar 29, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120939
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.