510(k) K072292 ยท NHJ Device, Positive Pressure Breathing, Intermittent
NEGAVENT PLUS PEGASO COUGH, MODEL: DA-3 PLUS
| Applicant | Dima Italia Srl, Boulder CO, US |
| Decision | Substantially Equivalent, Jan 7, 2008 |
| Received | Aug 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072292
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.