510(k) K800125 ยท CBK Ventilator, Continuous, Facility Use
VENTILATOR TEST LUNG
| Applicant | Bio-Med Devices, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 24, 1980 |
| Received | Jan 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800125
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.