510(k) K896375 ยท CAF Nebulizer (Direct Patient Interface)
PREEMICARE NEBUTECH NEBULIZER SYSTEM
| Applicant | Preemicare Corp., Houston TX, US |
| Decision | Substantially Equivalent, Oct 29, 1990 |
| Received | Nov 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896375
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.