ClearanceBrief
510(k) K230751 ยท QNP Gastrointesinal Lesion Software Detection System

EW10-EC02 Endoscopy Support Program

ApplicantFujifilm Corporation, Ashigara Kami-Gun, JP
DecisionSubstantially Equivalent, Dec 15, 2023
ReceivedMar 17, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230751

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.