FDA 510(k) clearance recorded for Deep Reasoning Ai's NeuroDR

FDA cleared NeuroDR, a radiology device from Deep Reasoning Ai, under the 510(k) pathway; the filing is listed under product code QIH and the radiology committee.

• The applicant is Deep Reasoning Ai, Inc., and the review committee is Radiology.
• The filing is listed under product code QIH.

Automated summary

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