ClearanceBrief
510(k) K894939 ยท FPD Tube, Feeding

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TRAY

ApplicantNorth American Sterilization & Packaging Co., Sparta NJ, US
DecisionSubstantially Equivalent, Dec 8, 1989
ReceivedAug 3, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894939

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.