Devilbiss Health Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Devilbiss Health Care, Inc. - FDA 510(k) Cleared Devices
29
Total
28
Cleared
0
Denied
Devilbiss Health Care, Inc. has 28 FDA 510(k) cleared anesthesiology devices. Based in Somerset, US.
Historical record: 28 cleared submissions from 1989 to 1997.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Devilbiss Health Care, Inc.
29 devices
Cleared
Jun 13, 1997
DEVILBISS 8650D
Anesthesiology
291d
Cleared
Apr 15, 1997
COMPRESSOR/NEBULIZER #3650
Anesthesiology
81d
Cleared
Oct 21, 1996
PULSE DOSE SERIES
Anesthesiology
214d
Cleared
Feb 08, 1996
MODEL #7354
Anesthesiology
349d
Cleared
Jan 31, 1996
MODEL 7355
Anesthesiology
246d
Cleared
Jan 30, 1996
JET NEBULIZER
Anesthesiology
260d
Cleared
Nov 09, 1995
5 LPM OXYGEN CONCENTRATOR
Anesthesiology
87d
Cleared
Sep 06, 1995
3 LPM OXYGEN CONCENTRATOR
Anesthesiology
128d
Cleared
Aug 24, 1995
DEVILBISS MODEL 5500
Anesthesiology
253d
Cleared
Apr 21, 1995
MODEL# 7500 SURVEYOR
Anesthesiology
214d
Cleared
Nov 10, 1994
CONTINUOUS POSITIVE AIRWAY PRESSURE CPAP SYSTEM
Anesthesiology
332d
Cleared
Sep 30, 1993
DEVILBISS MODEL 4650 COMPRESSOR NEUBULIZER
Anesthesiology
216d