FDA 510(k) Applications Submitted by AIRSEP CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020324	01/31/2002	LIFESTYLE OXYGEN CONCENTRATOR	AIRSEP CORP.
K012037	06/29/2001	HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009	AIRSEP CORP.
K983002	08/28/1998	MYSTIQUE ULTRASONIC NEBULIZER	AIRSEP CORP.
K960309	01/05/1996	AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)	AIRSEP CORP.
K943207	07/05/1994	NITELIFE BI-LEVEL CPAP	AIRSEP CORP.
K992283	07/07/1999	ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY	AIRSEP CORP.
K001579	05/22/2000	IMPULSE SELECT	AIRSEP CORP.
K962766	07/16/1996	AIRSEP IMPULSE	AIRSEP CORP.
K000963	03/24/2000	DA VINCHI EEG AND EMG/EP SYSTEMS	AIRSEP CORP.
K001013	03/29/2000	MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY	AIRSEP CORP.
K101154	04/23/2010	CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L	AIRSEP CORP.
K001467	05/10/2000	DA VINCHI EMG/EP ISA1004EP	AIRSEP CORP.
K080348	02/11/2008	OXISCAN II DATA MANAGEMENT SYSTEM	AIRSEP CORP.
K962865	07/23/1996	REMBRANDT SYSTEM	AIRSEP CORP.