510(k) K882694 ยท CBH Device, Fixation, Tracheal Tube
FIXATION DEVICE, TRACH TUBE
| Applicant | Bioseal, Brea CA, US |
| Decision | Substantially Equivalent, Aug 15, 1988 |
| Received | Jun 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882694
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.