510(k) K991788 ยท CAF Nebulizer (Direct Patient Interface)
SALTER LABS PEP DEVICE
| Applicant | Salter Labs, Arvin CA, US |
| Decision | Substantially Equivalent, Aug 6, 1999 |
| Received | May 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991788
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.