ClearanceBrief
510(k) K063061 ยท KNT Tubes, Gastrointestinal (And Accessories)

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

ApplicantViasys Medsystems, Wheeling IL, US
DecisionSubstantially Equivalent, Apr 2, 2007
ReceivedOct 5, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063061

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.