FDA 510(k) Applications Submitted by GN Hearing A/S

FDA 510(k) Number Submission Date Device Name Applicant
K180495 02/26/2018 Tinnitus Sound Generator Module GN Hearing A/S
K181586 06/15/2018 Tinnitus Sound Generator Module GN Hearing A/S
K213424 10/21/2021 Jabra Enhance Plus GN Hearing A/S
K193303 11/29/2019 Tinnitus Sound Generator Module GN Hearing A/S


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