Beckman is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beckman - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Beckman has 6 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 6 cleared submissions from 1989 to 1999. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Beckman Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beckman
6 devices
Cleared
Jun 01, 1999
MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY...
Immunology
13d
Cleared
May 21, 1997
SYNCHRON SYUSTEMS DAT DRUG FREE URINE CONTROL
Toxicology
23d
Cleared
Jan 27, 1994
P-AMYLASE CONTROL
Chemistry
84d
Cleared
Oct 22, 1990
SYNCHRON CX 7 CLINICAL ANALYZER
Chemistry
40d
Cleared
Oct 15, 1990
SYNCHRON CX4-CE
Chemistry
33d
Cleared
Aug 15, 1989
BECKMAN CHOLINESTERASE REAGENT KIT
Chemistry
98d