Airsep Corp. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Airsep Corp. has 17 FDA 510(k) cleared anesthesiology devices. Based in Buffalo, US.
Historical record: 17 cleared submissions from 1987 to 2011.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Mar 28, 2011
CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L
Anesthesiology
339d
Cleared
Oct 09, 2008
OXISCAN II DATA MANAGEMENT SYSTEM
Anesthesiology
241d
Cleared
Mar 13, 2002
LIFESTYLE OXYGEN CONCENTRATOR
Anesthesiology
41d
Cleared
Jan 17, 2002
HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009
Anesthesiology
202d
Cleared
Oct 20, 2000
DA VINCHI EEG AND EMG/EP SYSTEMS
Neurology
210d
Cleared
Aug 31, 2000
IMPULSE SELECT
Anesthesiology
101d
Cleared
Aug 01, 2000
DA VINCHI EMG/EP ISA1004EP
Neurology
83d
Cleared
May 16, 2000
MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
Neurology
48d
Cleared
Aug 27, 1999
ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
Neurology
51d
Cleared
Oct 16, 1998
MYSTIQUE ULTRASONIC NEBULIZER
Anesthesiology
49d
Cleared
Feb 28, 1997
AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)
Anesthesiology
420d
Cleared
Oct 25, 1996
REMBRANDT SYSTEM
Anesthesiology
94d