510(k) K840118 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
RHINOTHERM
| Applicant | Ascot Pharmaceuticals, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 13, 1984 |
| Received | Jan 11, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840118
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.