Medical Device Manufacturer · US , Washington , DC

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

16 submissions · 16 cleared · Since 1989

Total

Cleared

Denied

Colony Laboratories, Inc. has 16 FDA 510(k) cleared toxicology devices. Based in Washington, US.

Historical record: 16 cleared submissions from 1989 to 1989.

Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Colony 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 - Colony Laboratories, Inc.

16 devices

1-16 of 16

FPR AMIKACIN CALIBRATOR KIT

FPR GENTAMICIN CALIBRATOR KIT

FPR DIGOXIN CALIBRATOR KIT

FPR PHENYTOIN CALIBRATOR KIT

K894528 · DLG

Toxicology · 67d

Cleared Sep 18, 1989

FPR THEOPHYLLINE CALIBRATOR KIT

FPR TOBRAMYCIN CALIBRATOR KIT

K894532 · DLJ

Toxicology · 43d

Cleared Aug 28, 1989

FPR CARBAMAZEPINE KIT

K894519 · KLT

Toxicology · 39d

Cleared Aug 28, 1989

FPR CARBAMAZEPINE CALIBRATOR KIT

K894520 · DLJ

Toxicology · 39d

Cleared Aug 28, 1989

FPR PHENOBARBITAL KIT

K894525 · LGQ

Toxicology · 39d

Cleared Aug 28, 1989

FPR PHENOBARBITAL CALIBRATOR KIT

K894526 · DLJ

Toxicology · 39d

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

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

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