ClearanceBrief
510(k) K840036 ยท

FITEX

ApplicantBritt Corp., Inc., Chanhassen MN, US
DecisionSubstantially Equivalent, Oct 26, 1984
ReceivedJan 5, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840036

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.