ClearanceBrief
510(k) K132424 ยท KNT Tubes, Gastrointestinal (And Accessories)

METRIXCARE

ApplicantThe Metrix Company, Dubuque IA, US
DecisionSubstantially Equivalent, Feb 12, 2014
ReceivedAug 5, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132424

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.