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LumiraDx Submits First 510(k) Application to the FDA for COVID Ultra Test

June 30, 2023

LumiraDx submits a traditional 510 Dual Submission for LumiraDx SARS-CoV-2 Ag Ultra with CLIA Waiver for the commercial distribution at point of care of the LumiraDx Platform, including the LumiraDx...

City Of United Kingdom United States Carol Adiletto Francis Drug Administration Lumiradx Limited Nasdaq

Source: marketscreener.com

LumiraDx Five-Minute SARS-CoV-2 Ag Ultra Test Achieves CE Marking

May 19, 2022

Results in just 5 minutes from sample application, aids in fast clinical decision-making at point of care (POC), helping to inform treatment decisions and...

United Kingdom Ron Zwanziger Colleen Mcmillen Exchange Commission Head Of The Division Biology Pathology Montpellier University Hospital Center

Source: prnewswire.com

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Ultra Test News Today

LumiraDx Submits First 510(k) Application to the FDA for COVID Ultra Test

LumiraDx Five-Minute SARS-CoV-2 Ag Ultra Test Achieves CE Marking

Explore More Categories