Legacy MedSearch Insights
December 18, 2019
Clinical Study Utilizes the myTAIHEART Test to Monitor Cell-Free DNA Levels, 2-10 Days Post-Transplantation, in Pediatric Heart Transplant Recipients
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December 17, 2019
FDA Clears Two Siemens Healthineers CT Systems Dedicated for Radiation Therapy Planning
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December 16, 2019
FDA Approves Diffusion-Weighted Images for Elekta Unity, Expanding Options for Assessment During Therapy
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December 16, 2019
First Patient Enrolls in New Trial for Abiomed’s Impella Looks for Heart Failure Reduction
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December 12, 2019
Aptar’s Nasal Unidose Device Approved by U.S. FDA for First Nasal Rescue Treatment for Frequent Seizure Activity
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December 12, 2019
ImpediMed Receives FDA 510(k) Clearance of SOZO for Expanded Indication
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December 11, 2019
Beta Bionics Receives FDA Breakthrough Device Designation for the iLet Bionic Pancreas System
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December 10, 2019
MolecuLight Receives FDA 510(k) Clearance for its i:X Handheld Fluorescence Imaging Device for Wound Management
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December 10, 2019
Nihon Kohden Launches Life Scope SVM-7200 Series Vital Sign Monitor, a Portable, Easy-to-Use Monitor with Customizable Early Warning Scoring
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