510(k) K984085 ยท CAF Nebulizer (Direct Patient Interface)
RITEFLO SPACER
| Applicant | Aeromax Technologies, Inc., Phoenix AZ, US |
| Decision | Substantially Equivalent, Aug 5, 1999 |
| Received | Nov 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984085
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.