510(k) K834565 ยท BTS Tube, Bronchial (W/Wo Connector)
ENDOBRONCHIAL TWIN LUMEN TUBE
| Applicant | Portex, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1984 |
| Received | Dec 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834565
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.