ClearanceBrief
510(k) K080821 ยท BTR Tube, Tracheal (W/Wo Connector)

MICROCUFF PEDIATRIC ENDOTRACHEAL TUBE

ApplicantKimberly-Clark Corp., Roswell GA, US
DecisionSubstantially Equivalent, Apr 22, 2008
ReceivedMar 24, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080821

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.