510(k) K950930 ยท CBH Device, Fixation, Tracheal Tube
TRACHE-TITE
| Applicant | The Varner Group, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 22, 1995 |
| Received | Mar 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950930
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.