510(k) K780088 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
HYMIDIFIER
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Feb 2, 1978 |
| Received | Jan 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780088
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.