GeneralAI / InformaticsDevices & AI clearances

FDA Clears Cleerly LABS Image Processing Software

U.S. FDA2w ago

The U.S. FDA cleared Cleerly LABS (Cleerly, Inc.) under the 510(k) pathway for radiological image processing.

  • Pathway: 510(k) premarket notification.
  • Device classification: product code LLZ (Radiological Image Processing System).
  • Manufacturer: Cleerly, Inc.
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