ClearanceBrief
510(k) K920691 ยท CBH Device, Fixation, Tracheal Tube

THE LEWIS TUBE HOLDER

ApplicantR. Lewis, Inc., New Orleans LA, US
DecisionSubstantially Equivalent, Mar 18, 1992
ReceivedFeb 14, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920691

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.