510(k) K862238 ยท BTR Tube, Tracheal (W/Wo Connector)
BIVONA FOME-CUF LASER ENDOTRACHEAL TUBE
| Applicant | Bivona Medical Technologies, Gary IN, US |
| Decision | Substantially Equivalent, Oct 15, 1986 |
| Received | Jun 12, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862238
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.