510(k) K093617 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
VENTLAB 6000 SERIES HUMIDIFIER
| Applicant | Ventlab Corp., Mocksville NC, US |
| Decision | Substantially Equivalent, Jan 27, 2011 |
| Received | Nov 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093617
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.