510(k) K850711 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
INHALATION THERAPY NEBULIZER DEVICE
| Applicant | Med USA, Waltham MA, US |
| Decision | Substantially Equivalent, Jun 5, 1985 |
| Received | Feb 22, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850711
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.