Medical Device Manufacturer · US , Dallas , TX

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

9 submissions · 9 cleared · Since 1989

Total

Cleared

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.

Tudor Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tudor Laboratories, Inc.

9 devices

1-9 of 9

THYROXINE CALIBRATOR KIT

N-ACETYLPROCAINAMIDE (NAPA) CALIBRATOR KIT

K895572 · DLJ

Toxicology · 54d

Cleared Oct 25, 1989

N-ACETYLPROCAINAMIDE (NAPA) (FPIA) KIT

VALPROIC ACID (FPIA) KIT

K895569 · LEG

Toxicology · 27d

Cleared Sep 28, 1989

PRIMIDONE (FPIA) CALIBRATOR KIT

K895568 · DLJ

Toxicology · 22d

Cleared Sep 28, 1989

VALPROIC ACID (FPIA) CALIBRATOR KIT

K895570 · DLJ

Toxicology · 22d

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

FDA 510(k) Regulatory Record - Tudor Laboratories, Inc.

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