Medical Device Manufacturer · US , Mchenry , IL

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

23 submissions · 23 cleared · Since 1980

Total

Cleared

Denied

Utak Laboratories, Inc. has 23 FDA 510(k) cleared toxicology devices. Based in Mchenry, US.

Historical record: 23 cleared submissions from 1980 to 1991.

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

Utak 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 - Utak Laboratories, Inc.

23 devices

1-12 of 23

Cleared Apr 12, 1991

UTAK LABORATORIES TOXICOLOGY CONTROL

K903061 · LAS

Toxicology · 277d

Cleared Oct 06, 1988

TRACE ELEMENTS SERUM TOXICOLOGY CONTROL

K883147 · JJY

Toxicology · 72d

Cleared Nov 13, 1986

BENZODIAZEPINES TOXICOLOGY CONTROL

K862418 · LAS

Toxicology · 141d

Cleared Nov 13, 1986

SERUM VANCOMYCIN TOXICOLOGY CONTROL

K862419 · LAS

Toxicology · 141d

Cleared Nov 05, 1986

SERUM CLONAZEPAM TOXICOLOGY CONTROL

K862421 · LAS

Toxicology · 133d

Cleared Aug 04, 1986

UTAK-STABBS TOXICOLOGY CONTROL

K862420 · JJY

Toxicology · 40d

Cleared Jul 28, 1983

TRICYCLIC ANTIDEPRESSANTS

K831736 · DIF

Toxicology · 58d

Cleared Jul 26, 1983

AMOXAPINE 8-HYDRO-XYAMOXAPINE

CAFFINE TOXICOLOGY CONTROL

K831738 · LAS

Toxicology · 56d

Cleared Jul 26, 1983

FLURAZEPAM TOXICOLOGY CONTROL

K831741 · DIF

Toxicology · 56d

Cleared Jul 19, 1983

TRICYCLIC ANTIDEPRESSNATS VI

K831737 · DIF

Toxicology · 49d

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

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

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