510(k) K926161 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
RES Q AIR SYSTEM MODEL HT-1000
| Applicant | C.F. Electronics, Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Aug 26, 1993 |
| Received | Dec 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926161
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.