Medical Device Manufacturer · US , Mchenry , IL

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

19 submissions · 19 cleared · Since 1981

Total

Cleared

Denied

Windsor Laboratories, Inc. has 19 FDA 510(k) cleared toxicology devices. Based in Mchenry, US.

Historical record: 19 cleared submissions from 1981 to 1987.

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

Windsor 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 - Windsor Laboratories, Inc.

19 devices

1-12 of 19

Cleared Oct 28, 1987

CARBAMAZEPINE (FPIA) CALIBRATOR KIT

K873281 · DLJ

Toxicology · 72d

Cleared Sep 22, 1987

CARBAMAZEPINE FPIA FLUORES. POLARIZA. IMMUNOASSAY

DIGOXIN (FPIA) CALIBRATOR KIT

K870389 · DLJ

Toxicology · 61d

Cleared Apr 01, 1987

PHENOBARBITAL (FPIA) CALIBRATOR KIT

K870390 · DLJ

Toxicology · 61d

Cleared Jan 05, 1987

DIGOXIN FPIA FLUORESCENCE POLARIZATION IMMUNOASSAY

K864333 · KXT

Toxicology · 62d

Cleared Nov 10, 1986

PHENOBARBITAL-FPIA FLUORES. POLAR. IMMUNOASSAY KIT

K863625 · LGQ

Toxicology · 54d

Cleared Aug 29, 1986

AMIKACIN (FPIA) CALIBRATOR KIT

THEOPHYLLINE (FPIA) CALIBRATOR KIT

K861768 · JIS

Toxicology · 49d

Cleared Jun 25, 1986

GENTAMICIN (FPIA) CALIBRATOR KIT

K861769 · JIS

Toxicology · 49d

Cleared Jun 25, 1986

PHENYTOIN (FPIA) CALIBRATOR KIT

K861770 · JIS

Toxicology · 49d

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

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

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