ClearanceBrief
510(k) K232298 ยท OWB Interventional Fluoroscopic X-Ray System

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl

ApplicantCanon, Inc., Kawasaki, JP
DecisionSubstantially Equivalent, Apr 26, 2024
ReceivedAug 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232298

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.