FDA 510(k) Applications Submitted by RESOUND CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K984547	12/22/1998	DIGITAL LGOB PROCEDURE USING RESOUND, DIGITAL 5000 SERIES HEARING AIDS	RESOUND CORP.
K960052	01/04/1996	RESOUND PERSONAL HEARING SYSTEM BT2-ES, BT2-EV, & BT241	RESOUND CORP.
K960229	01/17/1996	RESOUND REAL EAR LOUDNESS MAPPING (RELM) SYSTEM	RESOUND CORP.
K970215	01/21/1997	AUDALLION II HEARING SYSTEM	RESOUND CORP.
K960680	02/20/1996	RESOUND PERSONAL HEARING SYSTEMS EDR ENCORE SERIES MODELS EDR-E, EDR-ES, EDR-EV, & EDR-P1	RESOUND CORP.
K960684	02/20/1996	HEARING AID - AIR CONDUCTION	RESOUND CORP.
K971605	05/01/1997	RESOUND ED4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION	RESOUND CORP.
K964115	10/15/1996	RESOUND CC4 PERSONAL HEARING SYSTEM	RESOUND CORP.
K974081	10/29/1997	RESOUND STEALTH CIC	RESOUND CORP.
K974257	11/13/1997	RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)	RESOUND CORP.
K955867	12/28/1995	RESOUND PERSONAL HEARING SYSTEM BT247	RESOUND CORP.
K964557	11/13/1996	RESOUND BT4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION	RESOUND CORP.