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Ann: HeraMED Receives FDA 510(k) Clearance for HeraBEAT Device, page-6

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    Receiving the 510(k) clearance for the HeraBEAT US device now allows that product to be commercially distributed throughout the United States. HeraMED will progress the device’s entry into the US market, as quickly as practicable.

    bagger today.
    the giant will wake up. this will be in over $1 on horizon.
    Last edited by Alby118: 18/11/19
 
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