510(k) K971981 ยท CAF Nebulizer (Direct Patient Interface)
LS SERIES 200 FLOVISION SYSTEM
| Applicant | Systam, Elfers FL, US |
| Decision | Substantially Equivalent, Dec 22, 1998 |
| Received | May 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971981
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.