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510(K)

CorticoMetrics's THINQ Receives the US FDA's 510(k) Clearance for MRI Brain Volumetric Reporting

CorticoMetrics's THINQ Receives the US FDA's 510(k) Clearance for MRI Brain Volumetric Reporting

  • November 26, 2020
Paige Receives the US FDA's 510(k) Clearance for its FullFocus Viewer to Use in Digital Pathology

Paige Receives the US FDA's 510(k) Clearance for its FullFocus Viewer to Use in Digital Pathology

  • July 21, 2020
Hyperfine Research Receives the US FDA's 510(k) Clearance for its World's First Bedside MRI system

Hyperfine Research Receives the US FDA's 510(k) Clearance for its World's First Bedside MRI system

  • February 19, 2020
Biofourmis' Biovitals Analytics Engine Receives FDA's 510(k) Clearance for Ambulatory Physiologic Monitoring

Biofourmis' Biovitals Analytics Engine Receives FDA's 510(k) Clearance for Ambulatory Physiologic Monitoring

  • October 7, 2019
Profound Medical's TULSA-PRO Receives the US FDA's 510(k) Clearance for Ablation of Prostate Tissue

Profound Medical's TULSA-PRO Receives the US FDA's 510(k) Clearance for Ablation of Prostate Tissue

  • August 16, 2019
Hologic & Cepheid's Diagnostic Tests Receive 510(k) Clearance for Extragenital Testing in Chlamydia and Gonorrhea

Hologic & Cepheid's Diagnostic Tests Receive 510(k) Clearance for Extragenital Testing in Chlamydia and Gonorrhea

  • May 24, 2019
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