ClearanceBrief
510(k) K894050 ยท JOH Tube Tracheostomy And Tube Cuff

MODIFIED DECANNULATION STOPPER

ApplicantPremier Medical, Philadelphia PA, US
DecisionSubstantially Equivalent, Aug 1, 1989
ReceivedJun 7, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894050

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.