Sunrise Medical Hhg, Inc. is one of 21679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sunrise Medical Hhg, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QUICKIE RHYTHM, DEVILBISS SLEEP RECORDER MODEL # RM60, DEVILBISS PD1000
10
Total
10
Cleared
0
Denied
Sunrise Medical Hhg, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Somerset, US.
Historical record: 10 cleared submissions from 1998 to 2008.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sunrise Medical Hhg, Inc.
10 devices
Cleared
Dec 23, 2008
QUICKIE RHYTHM
Physical Medicine
49d
Cleared
Jul 16, 2002
DEVILBISS SLEEP RECORDER MODEL # RM60
Anesthesiology
350d
Cleared
Jun 19, 2002
DEVILBISS PD1000
Anesthesiology
139d
Cleared
Jun 03, 2002
DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM
Anesthesiology
75d
Cleared
Jul 11, 2001
DEVILBISS 9000 SERIES CPAP, MODEL 9001
Anesthesiology
79d
Cleared
May 04, 2001
DEVILBISS HUMIDIFIER
Anesthesiology
161d
Cleared
Apr 21, 2000
DEVILBISS NEBULIZER MODEL 800
Anesthesiology
189d
Cleared
Nov 03, 1999
DEVILBISS 5 LITER OXYGEN CONCENTRATOR
Anesthesiology
167d
Cleared
Sep 25, 1998
DEVILBISS SUCTION UNIT
General & Plastic Surgery
86d
Cleared
Jul 17, 1998
DEVILBISS MODEL 6305D HEAVY DUTY AC ASPIRATOR
General & Plastic Surgery
73d