Tech-Co, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tech-Co, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST, VISUAL HCG PREGNANCY TEST, T4 EIA BEAD ASSAY
36
Total
36
Cleared
0
Denied
Tech-Co, Inc. has 36 FDA 510(k) cleared chemistry devices. Based in Troy, US.
Historical record: 36 cleared submissions from 1986 to 1996.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tech-Co, Inc.
36 devices
Cleared
Jun 28, 1996
IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST
Chemistry
1523d
Cleared
Oct 01, 1992
VISUAL HCG PREGNANCY TEST
Chemistry
84d
Cleared
Apr 17, 1992
T4 EIA BEAD ASSAY
Chemistry
58d
Cleared
Mar 24, 1992
DIRECT PREGNANCY TEST
Chemistry
35d
Cleared
Jul 10, 1990
POTASSIUM REAGENT SET
Chemistry
29d
Cleared
May 17, 1990
IRON/TOTAL IRON BINDING CAPACITY
Chemistry
44d
Cleared
Oct 13, 1988
ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
Chemistry
64d
Cleared
Oct 06, 1988
CHLORIDE
Chemistry
57d
Cleared
Oct 06, 1988
HEMOGLOBIN
Hematology
38d
Cleared
Jun 07, 1988
BILIRUBIN (DIRECT)
Chemistry
81d
Cleared
Jun 07, 1988
ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD)
Chemistry
81d
Cleared
May 27, 1988
GAMMA-GLUTAMYL TRANSFERASE
Chemistry
45d