Beckman-Diagnostic Systems Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beckman-Diagnostic Systems Group - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Beckman-Diagnostic Systems Group has 11 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 11 cleared submissions from 1993 to 1994. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Beckman-Diagnostic Systems Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beckman-Diagnostic Systems Group
11 devices
Cleared
Dec 12, 1994
I.D.-ZONE IMMUNOFIXATION ELECTROPHORESIS CONTROLS
Immunology
32d
Cleared
Dec 07, 1994
CX AMPHETAMINES REAGENT FOR SYNCHRON CX SYSTEMS
Toxicology
79d
Cleared
Dec 07, 1994
CX PHENCYCLIDINE REAGENT FOR SYNSCHRON CX SYSTEM
Toxicology
79d
Cleared
Nov 30, 1994
CX OPIATE REAGENT FOR SYNCHRON CX SYSTEMS
Toxicology
72d
Cleared
Nov 02, 1994
SYNCHRON CX3 DELTA
Chemistry
149d
Cleared
Jul 06, 1994
BECKMAN PANCREATIC AMYLASE (PAMY) REAGENT
Chemistry
307d
Cleared
Apr 26, 1994
BECKMAN DIRECT BILIRUBIN REAGENT
Chemistry
249d
Cleared
Apr 15, 1994
VIGIL PRX CHEMISTRY CONTROL
Toxicology
109d
Cleared
Nov 09, 1993
BECKMAN SYNCHRON LACTATE REAGENT
Chemistry
70d
Cleared
Oct 28, 1993
BECKMAN CHOLESTEROL REAGENT
Chemistry
70d
Cleared
Oct 27, 1993
BECKMAN CX AMMONIA/ALCOHOL CONTROL
Toxicology
47d