Medilab Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medilab Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Medilab Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1983 to 1984. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Medilab Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medilab Corp.
7 devices
Cleared
Jun 13, 1984
IMMU-TEC
Immunology
40d
Cleared
Jun 13, 1984
MONO-TEC
Immunology
40d
Cleared
Mar 30, 1984
MCS TOTAL PROTEIN REAGENT
Chemistry
66d
Cleared
Mar 30, 1984
MCS ALBUMIN REAGENT
Chemistry
66d
Cleared
Mar 05, 1984
LYSE-TEC
Hematology
41d
Cleared
Nov 03, 1983
PREGNA-TEC
Chemistry
70d
Cleared
Sep 12, 1983
PREGNA-TEC
Chemistry
45d