ClearanceBrief
510(k) K241389 ยท OPT Infrared Hematoma Detector

Infrascanner Model 2500 (Model 2500)

ApplicantInfrascan, Inc., Philadelphia PA, US
DecisionSubstantially Equivalent, Dec 12, 2024
ReceivedMay 15, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241389

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.