510(k) K931735 ยท BTR Tube, Tracheal (W/Wo Connector)
BLUE LINE(R) PDT(TM) PORTEX DIRECTIONAL TUBE
| Applicant | Smiths Industries Medical Systems, Inc., Keene NH, US |
| Decision | Substantially Equivalent, May 18, 1993 |
| Received | Apr 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931735
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.