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Hearing Innovations, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K013253 HISONIC-TRD TINNITUS RELIEF DEVICEKLW2002-04-05 View
510(k) K963745 MODEL WMR BTE HEARING INSTRUMENT (MODEL WMR)ESD1996-11-26 View
510(k) K951678 HI SONIC 2000 DIGITAL HEARING INSTRUMENTLXB1995-06-07 View
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