510(k) K980074 ยท CAF Nebulizer (Direct Patient Interface)
56 SERIES AEROSOL GENERATOR
| Applicant | Project Marketing, Cary NC, US |
| Decision | Substantially Equivalent, Jun 12, 1998 |
| Received | Jan 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980074
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.