Tago, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tago, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Tago, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1983 to 1984. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Tago, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tago, Inc.
8 devices
Cleared
Jun 01, 1984
TAGO FIFFU-GEN, OROSOMUCOID
Immunology
36d
Cleared
May 22, 1984
TAGO DIFFU-GEN C-REACTIVE PROTEIN
Chemistry
57d
Cleared
May 11, 1984
DIFFU-GEN APOLIPOPROTEIN A-I RADIAL -
Immunology
155d
Cleared
Mar 09, 1984
DIFFU-GEN HAPTOGLOBIN RADIAL IMMUNO
Immunology
38d
Cleared
Nov 21, 1983
TAGO DIFFU-GEN-APOLIPOPROTEIN B-100
Immunology
69d
Cleared
Mar 24, 1983
RA SCREENING TEST
Immunology
24d
Cleared
Mar 17, 1983
MONO SCREENING TEST
Immunology
27d
Cleared
Feb 09, 1983
HCG SCREENING TEST
Chemistry
22d