510(k) K962085 ยท CAF Nebulizer (Direct Patient Interface)
SALTER LABS 8990 SERIES NEBULIZER
| Applicant | Salter Labs, Arvin CA, US |
| Decision | Substantially Equivalent, Aug 26, 1996 |
| Received | May 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962085
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.