ClearanceBrief
510(k) K903579 ยท KNT Tubes, Gastrointestinal (And Accessories)

FLEXIFLO STOMATE DECOMPRESSION TUBE

ApplicantAbbott Laboratories, Columbus OH, US
DecisionSubstantially Equivalent, Nov 27, 1990
ReceivedAug 8, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903579

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.