Esa, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Esa, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Esa, Inc. has 7 FDA 510(k) cleared medical devices. Based in Bedford, US.
Historical record: 7 cleared submissions from 1987 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Esa, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Esa, Inc.
7 devices
Cleared
Jan 30, 2004
ESA PLASMA FREE METANEPHRINE ANALYSIS KIT
Chemistry
196d
Cleared
Sep 09, 1997
LEADCARE BLOOD LEAD TESTING SYSTEM
Toxicology
130d
Cleared
Dec 26, 1996
MODEL 5500 CEAS
Chemistry
86d
Cleared
Jan 11, 1994
MODEL 5500 CEAS
Chemistry
84d
Cleared
Jun 09, 1993
MODEL 5500 COULOCHEM ELECTRODE ARRAY SYSTEM
Chemistry
96d
Cleared
Sep 27, 1990
COULOCHEM II
Toxicology
66d
Cleared
Apr 13, 1987
NEUROCHEMICAL ANALYZER
Chemistry
130d