FDA 510(k) Applications Submitted by Julian Rutherford

FDA 510(k) Number Submission Date Device Name Applicant
K143395 11/26/2014 Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR Screener-Otocheck OAE+ABR, Otocheck OAE+ABR LE, Otocheck ABR Screener-Otodynamics ABR Upgrade Kit OTODYNAMICS, LTD.


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