510(k) K051522 ยท CBI Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
SILBRONCHO DOUBLE LUMEN TUBE
| Applicant | Fuji Systems Corp., Mccordsville IN, US |
| Decision | Substantially Equivalent, Aug 17, 2005 |
| Received | Jun 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051522
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.