Medical Device Manufacturer · US , Mchenry , IL

Anco Medical Reagents & Assoc. - FDA 510(k) Cleared Devices

26 submissions · 24 cleared · Since 1981

Total

Cleared

Denied

Anco Medical Reagents & Assoc. has 24 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 24 cleared submissions from 1981 to 1984.

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

Anco Medical Reagents & Assoc. 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 - Anco Medical Reagents & Assoc.

26 devices

1-12 of 26

Cleared Jul 27, 1984

SICKLE CELL STAT A/S HETEROZYGOUS-ERYTH

K842440 · JPK

Microbiology · 36d

Cleared Jul 28, 1983

SICKLE-HEME A/S CONTROLS & A/A CONTROL

ACID PHOSPHATASE REAGENT SET

K821526 · CKE

Chemistry · 20d

Cleared May 05, 1982

MEGNESIUM REAGENT KIT

K821102 · JGJ

Chemistry · 15d

Cleared Apr 26, 1982

ENZYMATIC CHOLESTEROL KIT

TOTAL LIPID REAGENT SET

K820500 · CFD

Chemistry · 16d

Cleared Jan 29, 1982

ALKALINE PHOSPHATASE REAGENT SET

K812837 · CJL

Chemistry · 112d

Cleared Dec 31, 1981

UREA NITROGEN REAGENT SET

K813415 · CDW

Chemistry · 24d

Cleared Dec 22, 1981

INORGANIC PHOSPHORUS REAGENT SET

K813400 · CEO

Pathology · 18d

Anco Medical Reagents & Assoc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Anco Medical Reagents & Assoc.

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