FDA 510(k) Applications Submitted by DAVID PREVES

FDA 510(k) Number	Submission Date	Device Name	Applicant
K972431	06/24/1997	MERIDIAN DSP	MICRO-EAR TECHNOLOGY, INC.
K964657	11/20/1996	SUPER K-AMP, EZ-COMPRESSION, TRIM-PRO, HF-PRO, ENVIRO-PRO, COMPRESSION-PRO, COMPRESSION 3000, HF 3000, OCTIVA, REFLEX HF	MICRO-EAR TECHNOLOGY, INC.
K962847	07/22/1996	MT10P, MT60-PP, MT60-AGC0, AND MT60	MICRO-TECH HEARING INSTRUMENTS
K970880	03/10/1997	POWER D, TRU 5, PERSONA, PERSONA CHOICE, MERIDIAN	MICRO-EAR TECHNOLOGY, INC.