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)
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