ClearanceBrief
510(k) K962240 ยท BTO Tube, Tracheostomy (W/Wo Connector)

MOORE TRACHEOSTOMY TUBE

ApplicantBoston Medical Products, Inc., Westborough MA, US
DecisionSubstantially Equivalent, Aug 15, 1996
ReceivedJun 11, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962240

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.