Medical Device Manufacturer · US , Mchenry , IL

Amresco, Inc. - FDA 510(k) Cleared Devices

39 submissions · 39 cleared · Since 1981

Total

Cleared

Denied

Amresco, Inc. has 39 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 39 cleared submissions from 1981 to 1991.

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

Amresco, 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 - Amresco, Inc.

39 devices

1-12 of 39

DIRECT BILIRUBIN REAGENT, 7776/7777/7576/7476/7176

AMRESCOCREAT KINASE REAGENT 7716/17,7516,7416,7116

K904004 · CGS

Chemistry · 104d

Cleared Dec 11, 1990

HDL-CHOLESTEROL PRECIPITANT 7773/7573/7473/7173

K905284 · LBR

Chemistry · 18d

Cleared Nov 28, 1990

GGT REAGENTS, 7738, 7739, 7538, 7438 & 7138

K905096 · JQB

Chemistry · 15d

Cleared Oct 12, 1990

DIAZO COLORIMENTRY DIRECT BILIRUBIN

K904381 · CIG

Chemistry · 16d

Cleared Oct 04, 1990

CREATINE PHOSPHOKINASE

BICARBONATE REAGENTS AMRESCO PRODUCT #4326020

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Amresco, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Amresco, Inc.

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