510(k) K790966 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
ULTRASONIC HUMIDIFIER
| Applicant | Hankscraft Div. of Gerber Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 11, 1979 |
| Received | May 22, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790966
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.