ClearanceBrief
510(k) K233030 ยท QIH Automated Radiological Image Processing Software

BoneMRI

ApplicantMriguidance B.V., Utrecht, NL
DecisionSubstantially Equivalent, Mar 1, 2024
ReceivedSep 25, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233030

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.