Atrion Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atrion Medical Products, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Atrion Medical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Arab, US.
Historical record: 9 cleared submissions from 1997 to 2006.
Browse the FDA 510(k) cleared devices submitted by Atrion Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Atrion Medical Products, Inc.
9 devices
Cleared
Jul 12, 2006
QL LOCKING SYRINGE
Cardiovascular
124d
Cleared
May 25, 2005
ATRION NEEDLEVISE LARGE-BORE SHARPS SECURING DEVICE
General Hospital
183d
Cleared
Jun 16, 2004
ATRION EPIDURAL ANESTHESIA KIT WITH ATRION NEEDLEVISE SHARPS SECURING SYSTEM
Anesthesiology
44d
Cleared
Mar 03, 2004
ATRION MEDICAL QL INFLATION DEVICE
Gastroenterology & Urology
174d
Cleared
Apr 25, 2002
ATRION MEDICAL QL FLUID DISPENSING SYRINGE
Cardiovascular
84d
Cleared
Jan 16, 1998
ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET
Ophthalmic
183d
Cleared
Jan 08, 1998
ATRION MEDICAL COATED LACRIMAL INTUBATION SET
Ophthalmic
90d
Cleared
Oct 10, 1997
ATRION MEDICAL BALLOON CATHETER INFLATION DEVICE
Gastroenterology & Urology
60d
Cleared
May 23, 1997
ATRION MEDICAL AUTOGENOUS TISSUE COLLECTOR
Dental
58d