510(k) K060094 ยท BTR Tube, Tracheal (W/Wo Connector)
ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES
| Applicant | Arcadia Medical Corporation, Schaumburg IL, US |
| Decision | Substantially Equivalent, May 8, 2006 |
| Received | Jan 12, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060094
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.