ClearanceBrief
510(k) K962389 ยท BTR Tube, Tracheal (W/Wo Connector)

EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

ApplicantUnomedical Sdn Bhd, Tarpon Springs FL, US
DecisionSubstantially Equivalent, Nov 21, 1996
ReceivedJun 20, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962389

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.