510(k) K901785 ยท CBK Ventilator, Continuous, Facility Use
NEWPORT WAVE VENTILATOR MODEL E200
| Applicant | Newport Medical Instruments, Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Aug 10, 1990 |
| Received | Apr 18, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901785
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.