510(k) K024344 ยท CBK Ventilator, Continuous, Facility Use
PNEUTON VENTILATOR
| Applicant | Airon Corporation, Melbourne FL, US |
| Decision | Substantially Equivalent, Jun 3, 2003 |
| Received | Dec 27, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024344
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.