GeneralDevices & AI clearances

Curemetrix cmAngio V2.0 gains FDA 510(k) clearance

U.S. FDA2w ago

The FDA has cleared Curemetrix, Inc.'s cmAngio® V2.0 via the 510(k) pathway, classifying it as a radiology image processing system (product code QIH).

  • Clearance granted under product code QIH (Radiology Committee).
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