ClearanceBrief
510(k) K895285 ยท GBZ Catheter, Cholangiography

MENTOR DUCTAL CATHETERS

ApplicantMentor Corp., Goleta CA, US
DecisionSubstantially Equivalent, Oct 17, 1989
ReceivedAug 24, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895285

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.