Draeger Medical, Inc. - FDA 510(k) Cleared Devices
78
Total
77
Cleared
0
Denied
Draeger Medical, Inc. has 77 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 77 cleared submissions from 1977 to 2004.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
78 devices
Cleared
Nov 26, 2004
PRIMUS US
Anesthesiology
63d
Cleared
Oct 08, 2004
FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEM
Anesthesiology
31d
Cleared
Sep 23, 2004
D-VAPOR
Anesthesiology
31d
Cleared
Aug 31, 2004
FABIUS GS ANESTHESIA SYSTEM
Anesthesiology
28d
Cleared
Jul 08, 2004
MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM
Anesthesiology
22d
Cleared
Jun 17, 2004
MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR
Anesthesiology
77d
Cleared
Apr 26, 2004
NARKOMED 6400, MODEL NM6400
Anesthesiology
173d
Cleared
Mar 17, 2004
MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM
Anesthesiology
384d
Cleared
Jul 15, 2003
FABIUS TIRO ANESTHESIA SYSTEM
Anesthesiology
71d
Cleared
Aug 29, 2002
NARKOMED MRI-2 ANESTHESIA SYSTEM, MODEL NM-MRI-2
Anesthesiology
69d
Cleared
Feb 22, 2002
FABIUS GS ANESTHESIA SYSTEM, MODEL FABIUS GS
Anesthesiology
290d
Cleared
Jan 17, 2002
VAMOS ANESTHETIC GAS MONITOR
Anesthesiology
191d
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