510(k) K932647 ยท BTR Tube, Tracheal (W/Wo Connector)
WIRE REINFORCED ENDOTRACHEAL TUBE
| Applicant | Vitaid, Ltd., Lewiston NY, US |
| Decision | Substantially Equivalent, Nov 2, 1993 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932647
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.