Essex Cryogenics of Missouri, Inc. is one of 18369 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Essex Cryogenics of Missouri, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OXYGEN GENERATOR LIQUEFIER - (OGL), BACKPACK MEDICAL OXYGEN SYSTEM, NEXT GENERATION PORTABLE THERAPEUTIC LIQUID OXYGEN SYSTEM
5
Total
5
Cleared
0
Denied
Essex Cryogenics of Missouri, Inc. has 5 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 5 cleared submissions from 1988 to 2014. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Essex Cryogenics of Missouri, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Essex Cryogenics of Missouri, Inc.
5 devices
Cleared
Feb 21, 2014
OXYGEN GENERATOR LIQUEFIER - (OGL)
Anesthesiology
238d
Cleared
Jul 11, 2007
BACKPACK MEDICAL OXYGEN SYSTEM
Anesthesiology
33d
Cleared
Mar 22, 2004
NEXT GENERATION PORTABLE THERAPEUTIC LIQUID OXYGEN SYSTEM
Anesthesiology
179d
Cleared
Sep 11, 2002
PORTABLE THERAPEUTIC OXYGEN CONCENTRATION SYSTEM (PTOCS)
Anesthesiology
30d
Cleared
Apr 14, 1988
PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT
Anesthesiology
90d