Nordiclab Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nordiclab Intl. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Nordiclab Intl. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1979 to 1980. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Nordiclab Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nordiclab Intl.
8 devices
Cleared
Sep 26, 1980
NORDICLAB PROSTATIC ACID PHOSPHATASE RIA
Chemistry
38d
Cleared
Sep 16, 1980
NORDICLAB FERRITIN IRMA TEST
Immunology
28d
Cleared
May 14, 1980
NORDICLAB ESTRADIOL RIA TEST
Chemistry
23d
Cleared
May 14, 1980
NORDICLAB TESTOSTERONE RIA TEST
Chemistry
23d
Cleared
May 14, 1980
NORDICLAB PROGESTERONE RIA TEST
Chemistry
23d
Cleared
Nov 13, 1979
NORDICLAB TOTAL ESTRIOL RIA TEST
Chemistry
13d
Cleared
Jan 17, 1979
IRMA TEST, NORDICLAB FERRITIN
Microbiology
26d
Cleared
Jan 10, 1979
RIA TEST, NORDICALB HPL
Immunology
23d