ClearanceBrief
510(k) K080253 ยท KGC Tube, Gastro-Enterostomy

KIMBERLY-CLARK INTRODUCER KITS

ApplicantKimberly-Clark Corp., Roswell GA, US
DecisionUnknown, Feb 26, 2008
ReceivedJan 31, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080253

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.