ClearanceBrief
510(k) K980305 ยท KNT Tubes, Gastrointestinal (And Accessories)

AMT BUTTON REPLACEMENT GASTROSTOMY DEVICE

ApplicantApplied Medical Technology, Inc., Cleveland OH, US
DecisionSubstantially Equivalent, Apr 16, 1998
ReceivedJan 27, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980305

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.