ClearanceBrief
510(k) K020379 ยท KNT Tubes, Gastrointestinal (And Accessories)

PPD BALLOON DILATATION CATHETER

ApplicantTelemed Systems, Inc., Hudson MA, US
DecisionSubstantially Equivalent, May 6, 2002
ReceivedFeb 5, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020379

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.