ClearanceBrief
510(k) K842808 ยท KNT Tubes, Gastrointestinal (And Accessories)

URITROL-M

ApplicantThe Washington Group, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Nov 16, 1984
ReceivedJul 18, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842808

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.