510(k) K915603 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
VIROTHERM HUMIDIFIER
| Applicant | Virotherm Laboratory, Saratoga CA, US |
| Decision | Substantially Equivalent, Oct 22, 1992 |
| Received | Dec 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915603
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.