510(k) K122705 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
HUMICARE D900
| Applicant | Grundler GmbH, San Diego CA, US |
| Decision | Substantially Equivalent, May 21, 2013 |
| Received | Sep 4, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122705
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.