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Brief: Duearity Submits FDA 510(K) Clearance Application For Tinearity G1

Dec 12 (Reuters) - Duearity AB  DUEAR.ST :
    * SUBMITS FDA APPLICATION FOR 510(K) CLEARANCE
    * APPLICATION COVERS CO'S TINNITUS PRODUCT TINEARITY G1
    * SAYS GOAL IS TO RECEIVE DECISION IN FIRST HALF OF 2023

Source text for Eikon:  ID:nMFN7kL552 
Further company coverage:  DUEAR.ST 
 (Gdansk Newsroom)
 ((gdansk.newsroom@thomsonreuters.com;))

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