Technia Diagnostics , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Technia Diagnostics , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Technia Diagnostics , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1979 to 1986. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Technia Diagnostics , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Technia Diagnostics , Ltd.
9 devices
Cleared
Jun 10, 1986
AUTOFLUOR V
Immunology
20d
Cleared
Sep 16, 1980
T3(125) RADIOIMMUNOASSAY KIT
Chemistry
46d
Cleared
Jun 20, 1980
DIGOXIN RADIOIMMUNOASSAY KIT
Toxicology
32d
Cleared
Jun 09, 1980
CORTISOL RADIOIMMUNOASSAY KIT
Chemistry
21d
Cleared
Aug 16, 1979
T3 UPTAKE RADIOIMMUNOASSAY KIT
Chemistry
27d
Cleared
Jun 28, 1979
HPL RIA KIT
Chemistry
45d
Cleared
May 03, 1979
THYROXINE RIA KIT
Chemistry
51d
Cleared
Feb 28, 1979
RIA KIT, VITAMIN B12
Chemistry
85d
Cleared
Jan 26, 1979
GENTAMICIN FLUROIMMUNASSAY KIT
Toxicology
52d