510(k) K953206 ยท CAF Nebulizer (Direct Patient Interface)
DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)
| Applicant | Dhd Diemolding Healthcare Div., Wampsville NY, US |
| Decision | Substantially Equivalent, Aug 28, 1995 |
| Received | May 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953206
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.