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  2. Abbott (ABT) CE-Marked Panbio Test Now Widely Offered ... - AOL

    www.aol.com/news/abbott-abt-ce-marked-panbio...

    Abbott's (ABT) Panbio COVID-19 Antigen Self-Test is expected to facilitate mass screenings and aid in resumption of daily life activities with the gradual reopening of economies worldwide.

  3. Free at-home COVID-19 tests will be available again soon ...

    www.aol.com/free-home-covid-19-tests-163432725.html

    A positive result on an Abbott COVID test taken by a Columbus-area resident in July. More: COVID-19 vaccines are updated and ready for fall, FDA says.

  4. Abbott Laboratories (ABT) Q4 2024 Earnings Call Transcript - AOL

    www.aol.com/abbott-laboratories-abt-q4-2024...

    Image source: The Motley Fool. Abbott Laboratories (NYSE: ABT) Q4 2024 Earnings Call Jan 22, 2025, 9:30 a.m. ET. Contents: Prepared Remarks. Questions and Answers. Call Participants

  5. COVID-19 rapid antigen test - Wikipedia

    en.wikipedia.org/wiki/COVID-19_rapid_antigen_test

    Health Canada approved its first COVID-19 RAT in October 2020, the Abbott Panbio test. [49] As of October 2020, there were questions in the US as to whether manufacturing capacity could keep up with the potential demand for hundreds of millions of RATs. [50] [51] RATs began to be rolled out across Portuguese schools and care homes. [52]

  6. Abbott Laboratories - Wikipedia

    en.wikipedia.org/wiki/Abbott_Laboratories

    Abbott Laboratories is an American multinational medical devices and health care company with headquarters in Abbott Park, Illinois, in the United States. The company was founded by Chicago physician Wallace Calvin Abbott in 1888 to formulate known drugs; today, it sells medical devices, diagnostics, branded generic medicines and nutritional products.

  7. Development of COVID-19 tests - Wikipedia

    en.wikipedia.org/wiki/Development_of_COVID-19_tests

    On 8 May, the FDA granted its first EUA for antigen test: "Sofia 2 SARS Antigen FIA" by Quidel Corp. [88] [89] The FDA announced on 14 May a review of 15 adverse event reports about the Abbott ID Now device for low sensitivity. [90] On 21 May, researchers at Ben-Gurion University in Israel reported a one-minute coronavirus test with 90% ...

  8. Abbott’s BinaxNOW COVID-19 Ag Self Test Cleared For ... - AOL

    www.aol.com/news/abbott-binaxnow-covid-19-ag...

    Abbott’s BinaxNOW COVID-19 Ag Self Test, which was designed to detect COVID-19 infection, has been authorized for emergency use by the US Food and Drug Administration (FDA). The approval permits ...

  9. COVID-19 testing in the United States - Wikipedia

    en.wikipedia.org/wiki/COVID-19_testing_in_the...

    The patient's test was delayed for four days because he had not qualified for a test under the initial federal testing criteria. [9] By February 27, fewer than 4,000 tests had been conducted in the U.S. [ 10 ] Although academic laboratories and hospitals had developed their own tests, they were not allowed to use them until February 29, when ...