ClearanceBrief
510(k) K924306 ยท KNT Tubes, Gastrointestinal (And Accessories)

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY

ApplicantUnited States Endoscopy Group, Inc., Mentor OH, US
DecisionSubstantially Equivalent, May 15, 1995
ReceivedAug 26, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924306

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.