ClearanceBrief
510(k) K822794 ยท CBH Device, Fixation, Tracheal Tube

RESPIRONICS ENDO TUBE CONTROL SYS

ApplicantRespironics, Inc., Monroeville PA, US
DecisionSubstantially Equivalent, Oct 22, 1982
ReceivedSep 16, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822794

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.