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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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