ClearanceBrief
510(k) K022212 ยท JOH Tube Tracheostomy And Tube Cuff

PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS

ApplicantMentor Medical Limited, Hyth, Kent, GB
DecisionSubstantially Equivalent, Mar 21, 2003
ReceivedJul 8, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022212

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.