ClearanceBrief
510(k) K843790 ยท CBH Device, Fixation, Tracheal Tube

TRACHEAL TUBE FIXATION DEVICE

ApplicantLaerdal California, Inc., Long Beach CA, US
DecisionSubstantially Equivalent, Mar 11, 1985
ReceivedSep 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843790

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.