ClearanceBrief
510(k) K800078 ยท

BRIOX MODEL-AEROMIST

ApplicantBriox Technologies, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 5, 1980
ReceivedJan 14, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800078

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.