Livonia Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Livonia Diagnostics, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Livonia Diagnostics, Inc. has 16 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1984 to 1985.
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 - Livonia Diagnostics, Inc.
16 devices
Cleared
Jun 10, 1985
SERUM IRON/VIBC REAGENT SET
Toxicology
21d
Cleared
Nov 27, 1984
SGPT REAGENT SET
Chemistry
22d
Cleared
Nov 27, 1984
SGOT REAGENT SET
Chemistry
20d
Cleared
Nov 20, 1984
ALKALINE PHOSPHATASE REAGENT SET
Chemistry
19d
Cleared
Nov 13, 1984
UREA NITROGEN REAGENT SET
Chemistry
20d
Cleared
Nov 09, 1984
INORGANIC PHOSPHORUS REAGENT SET
Chemistry
14d
Cleared
Nov 02, 1984
HDL PRECIPATATING REAGENT SET
Chemistry
30d
Cleared
Oct 30, 1984
MAGNESIUM REAGENT SET
Chemistry
27d
Cleared
Oct 30, 1984
TOTAL CALCIUM REAGENT SET
Chemistry
27d
Cleared
Oct 30, 1984
CREATININE REAGENT SET
Chemistry
15d
Cleared
Oct 30, 1984
URIC ACID REAGENT SET
Chemistry
11d
Cleared
Oct 11, 1984
ALBUMIN REAGENT SET
Chemistry
10d
Cleared
Oct 01, 1984
TOTAL PROTEIN REAGENT SET
Chemistry
10d
Cleared
Sep 28, 1984
ENZYMATIC CHOLESTEROL KIT
Chemistry
43d
Cleared
Sep 28, 1984
GLUCOSE OXIDASE ENZYMATIC REAGENT SET
Chemistry
21d
Cleared
Jul 20, 1984
SICKLE CELL REAGENT SET
Hematology
35d