ClearanceBrief
510(k) K073718 ยท KGC Tube, Gastro-Enterostomy

MEDLINE GASTROSTOMY TUBE

ApplicantMedline Industries, Inc., Mundelein IL, US
DecisionSubstantially Equivalent, Mar 19, 2008
ReceivedDec 31, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K073718

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.