ClearanceBrief
510(k) K821456 ยท BTR Tube, Tracheal (W/Wo Connector)

ENDOTRACHEAL TUBE

ApplicantLife-Line Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 17, 1982
ReceivedMay 14, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821456

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.