ClearanceBrief
510(k) K942395 ยท CBH Device, Fixation, Tracheal Tube

ENDOTRACHEAL TUBE HOLDER

ApplicantS.T.I. Medical Products Corp., Newport Beach CA, US
DecisionSubstantially Equivalent, Jun 30, 1994
ReceivedMay 19, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942395

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.