Drager, Inc. - FDA 510(k) Cleared Devices
20
Total
15
Cleared
0
Denied
Drager, Inc. has 15 FDA 510(k) cleared anesthesiology devices. Based in Pittsburgh, US.
Historical record: 15 cleared submissions from 1991 to 1999.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
20 devices
Cleared
Aug 24, 1999
ATC OPTION FOR EVITA 2 DURA AND EVITA 4
Anesthesiology
20d
Cleared
Jan 22, 1999
DRAGER OXYLOG 2000
Anesthesiology
30d
Cleared
Dec 07, 1998
NEOFLOW OPTION MODEL NUMBERS 8413563, 8411900
Anesthesiology
84d
Cleared
Oct 29, 1998
MEDICAL AIR COMPRESSOR, MODEL # 8413419
Anesthesiology
80d
Cleared
Sep 04, 1998
EVITA 4 (8411900)
Anesthesiology
197d
Cleared
Jun 17, 1998
BABYLOG 8000 PLUS
Anesthesiology
223d
Cleared
Oct 03, 1997
BABYTHERM 8004 BABYTHERM 8010
General Hospital
186d
Cleared
Aug 26, 1997
EVITA 2 DURA
Anesthesiology
222d
Cleared
Apr 25, 1997
DRAGER INCUBATOR 8000 IC
General Hospital
597d
Cleared
Dec 13, 1996
EVITA 4
Anesthesiology
226d
Cleared
Nov 05, 1996
OPTIONAL DISPLAY AND SOFTWARE FOR DRAGER VENTILATORS
Anesthesiology
617d
Cleared
Sep 16, 1996
DRAGER MICRO VENT
Anesthesiology
433d
Cleared
Feb 09, 1996
DRAGER INFANT RADIANT WARMERN RH600
General Hospital
199d
Cleared
Dec 01, 1995
DRAGER PT4000 PHOTOTHERAPY SYSTEM
General Hospital
58d
Cleared
Aug 25, 1995
OXYLOG 2000
Anesthesiology
400d
Cleared
Apr 28, 1995
BABYTHERM 8000 WB
Physical Medicine
172d
Cleared
Mar 24, 1995
DRAGER MEDICAL AIR COMPRESSOR
Anesthesiology
11d
Cleared
Apr 19, 1994
BABYLOG 8000 INFANT VENTILATOR
Anesthesiology
491d
Cleared
Jan 10, 1994
EVITA
Anesthesiology
467d
Cleared
Jun 10, 1991
BABYLOG 8000 INFANT VENTILATOR
Anesthesiology
332d