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VasQ TM has a Breakthrough Device designation effective June 5, 2020, and De Novo classification from FDA effective September 26, 2023, for the indication covered by the Breakthrough Device designation

Research from her team found that a delayed injection site reaction occurred in less than 1% of participants (244 people) after the first dose of the Moderna vaccine and only 0.2% participants (68 people) after the second dose