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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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