Los Alamos Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Los Alamos Diagnostics - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Los Alamos Diagnostics has 7 FDA 510(k) cleared medical devices. Based in Los Alamos, US.
Historical record: 7 cleared submissions from 1987 to 1989. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Los Alamos Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Los Alamos Diagnostics
7 devices
Cleared
Nov 30, 1989
MODIFIED MODEL 535(TM) LUMINOMETER
Chemistry
41d
Cleared
Sep 07, 1988
RESUBMITTED UTISCREEN(TM) BACTERIAL ATP TEST
Microbiology
29d
Cleared
Aug 29, 1988
LAD MODEL 633 LUMINOMETER
Chemistry
66d
Cleared
Apr 28, 1988
MODIFIED UTISCREEN(TM) BACTERIAL ATP TEST SYSTEM
Microbiology
23d
Cleared
Nov 27, 1987
LAD MODEL 735 LUMINOMETER
Chemistry
38d
Cleared
Feb 13, 1987
UTISCREEN(R) BACTERIAL ATP TEST
Microbiology
109d
Cleared
Jan 13, 1987
LAD MODEL 535 LUMINOMETER
Chemistry
78d