510(k) K960795 ยท BTR Tube, Tracheal (W/Wo Connector)
VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE
| Applicant | Vygon Corp., West Cadwell NJ, US |
| Decision | Substantially Equivalent, May 22, 1996 |
| Received | Feb 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960795
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.