510(k) K881935 ยท CAF Nebulizer (Direct Patient Interface)
MICROCIRRUS MEDICAL NEBULIZER
| Applicant | Dhd Medical Products Div. Diemolding Corp., Canastota NY, US |
| Decision | Substantially Equivalent, Jun 22, 1988 |
| Received | May 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881935
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.