510(k) K831646 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
SONIC MIST ULTRASONIC HUMIDIFIER
| Applicant | Douglas Products, Walker MI, US |
| Decision | Substantially Equivalent, Jul 12, 1983 |
| Received | May 19, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831646
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.