510(k) K880923 ยท CBK Ventilator, Continuous, Facility Use
PATIENT VENTILATOR ISOLATOR
| Applicant | Dryden Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 6, 1988 |
| Received | Mar 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880923
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.