Medical Device Manufacturer · US , Dallas , TX

Tudor Laboratories, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1989

9

Total

9

Cleared

0

Denied

Tudor Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Dallas, US.

Historical record: 9 cleared submissions from 1989 to 1992. Primary specialty: Toxicology.

Browse the FDA 510(k) cleared devices submitted by Tudor Laboratories, Inc. Filter by specialty or product code using the sidebar.

9 devices

1–9 of 9

THYROXINE (FPIA) KIT

K921904 · KLI Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine · Chemistry

THYROXINE CALIBRATOR KIT

K921903 · JIS Calibrator, Primary · Chemistry

DIGITOXIN (FPIA) KIT

K913240 · LFM Enzyme Immunoassay, Digitoxin · Toxicology

N-ACETYLPROCAINAMIDE (NAPA) CALIBRATOR KIT

K895572 · DLJ Calibrators, Drug Specific · Toxicology

N-ACETYLPROCAINAMIDE (NAPA) (FPIA) KIT

K895571 · LAN Enzyme Immunoassay, N-acetylprocainamide · Toxicology

PRIMIDONE (FPIA) KIT

K895567 · LFT Fluorescent Immunoassay, Primidone · Toxicology

VALPROIC ACID (FPIA) KIT

K895569 · LEG Enzyme Immunoassay, Valproic Acid · Toxicology

PRIMIDONE (FPIA) CALIBRATOR KIT

K895568 · DLJ Calibrators, Drug Specific · Toxicology

VALPROIC ACID (FPIA) CALIBRATOR KIT

K895570 · DLJ Calibrators, Drug Specific · Toxicology