FDA 510(k) Applications Submitted by Chris Roerig

FDA 510(k) Number Submission Date Device Name Applicant
K150163 01/26/2015 Otowave 202 Portable Tympanometer AMPLIVOX, LTD.
K171265 05/01/2017 Otowave 302 Portable Tympanometer Amplivox Ltd


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