In Vitro Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In Vitro Diagnostics, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
In Vitro Diagnostics, Inc. has 15 FDA 510(k) cleared chemistry devices. Based in Shelton, US.
Historical record: 15 cleared submissions from 1985 to 1990.
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 - In Vitro Diagnostics, Inc.
15 devices
Cleared
Feb 23, 1990
THYROID STIMULATING HORMONE-EIA-XT
Chemistry
79d
Cleared
Feb 13, 1990
DIGOXIN-EIA-XT
Toxicology
69d
Cleared
Feb 13, 1990
LUTEINIZING HORMONE-EIA-XT
Chemistry
69d
Cleared
Jan 30, 1990
VITRO T4-EIA-XT
Chemistry
55d
Cleared
Jan 18, 1990
T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT
Chemistry
37d
Cleared
Jan 11, 1990
FOLLICLE STIMULATING HORMONE-EIA-XT
Chemistry
36d
Cleared
Nov 23, 1987
REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801
Hematology
63d
Cleared
May 28, 1987
FLAME PHOTOMETER STANDARD #60081 120 NA/2K
Chemistry
65d
Cleared
May 28, 1987
FLAME PHOTOMETER STANDARD #60082 140 NA/5K
Chemistry
65d
Cleared
May 28, 1987
FLAME PHOTOMETER STANDARD #60083 160 NA/8K
Chemistry
65d
Cleared
May 28, 1987
LITHIUM INTERNAL STANDARD 1 MEQ/L #60085
Chemistry
65d
Cleared
May 28, 1987
CESIUM DILUENT 1.5 MMOL CS/L #60087
Chemistry
65d