FDA 510(k) Applications Submitted by KRISTA M BUCKLES, M.A.

FDA 510(k) Number Submission Date Device Name Applicant
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.
K980533 02/11/1998 ERO-SCAN OTOACOUSTIC EMISSIONS TEST INST. (ER34) ETYMOTIC RESEARCH
K964557 11/13/1996 RESOUND BT4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION RESOUND CORP.


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