ClearanceBrief
510(k) K810392 ยท KNT Tubes, Gastrointestinal (And Accessories)

OESOPHAGEAL THERAPY KIT

ApplicantKeymed, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 31, 1981
ReceivedFeb 17, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810392

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.