ClearanceBrief
510(k) K093186 ยท BTR Tube, Tracheal (W/Wo Connector)

AMBU ASCOPE AND MONITOR

ApplicantAmbu A/S, Glen Burnie MD, US
DecisionSubstantially Equivalent, Apr 16, 2010
ReceivedOct 9, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093186

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.