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Flowflex® Plus COVID-19 Home Test

ACON Laboratories, Inc. · Class II · Cleared Apr 19, 2024

K-numberK233373
Device nameFlowflex® Plus COVID-19 Home Test
ApplicantACON Laboratories, Inc.
Product codeQYT
Device classClass II
Decision dateApr 19, 2024
DecisionSubstantially Equivalent
Regulation866.3984
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View the full FDA submission: accessdata.fda.gov

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