ClearanceBrief
510(k) K192259 ยท PSY Whole Slide Imaging System

Philips IntelliSite Pathology Solution

ApplicantPhilips Electronics Nederland B.V., Best, NL
DecisionSubstantially Equivalent, Sep 20, 2019
ReceivedAug 21, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K192259

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.