ClearanceBrief
510(k) K904801 ยท KGC Tube, Gastro-Enterostomy

ORION LIFE SYSTEMS REPLACEMENT GASTROSTOMY TUBE

ApplicantOrion Life Systems, Inc., Wheeling IL, US
DecisionSubstantially Equivalent, Jan 16, 1991
ReceivedOct 24, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904801

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.