510(k) K113333 ยท BTR Tube, Tracheal (W/Wo Connector)
KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS
| Applicant | Kimberly-Clark Corporation, Roswell GA, US |
| Decision | Substantially Equivalent, May 11, 2012 |
| Received | Nov 14, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113333
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.