510(k) K862171 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)
MP-500 ELECTRONIC NEBULIZER
| Applicant | The Timeter Group, Lancaster PA, US |
| Decision | Substantially Equivalent, Jul 14, 1986 |
| Received | Jun 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862171
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.