ClearanceBrief
510(k) K973892 ยท KNT Tubes, Gastrointestinal (And Accessories)

RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)

ApplicantRusch Intl., Jeffrey NH, US
DecisionSubstantially Equivalent, May 18, 1998
ReceivedOct 14, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973892

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.