FDA 510(k) Applications Submitted by AMPLIVOX, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K150163 01/26/2015 Otowave 202 Portable Tympanometer AMPLIVOX, LTD.
K081841 06/30/2008 AMPLIVOX OTOWAVE 102 HAND HELD PORTABLE TYMPANOMETER AMPLIVOX, LTD.


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