Medical Device Manufacturer · US , Mchenry , IL

Reagent Laboratory, Inc. - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1984

Total

Cleared

Denied

Reagent Laboratory, Inc. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1984 to 1986. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Reagent Laboratory, Inc. Filter by specialty or product code using the sidebar.

Reagent Laboratory, 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 - Reagent Laboratory, Inc.

19 devices

1-12 of 19

Cleared Oct 21, 1986

SOLUTION B- NA 50MEQ/L, K 40 MEQ/L

POTASSIUM HYDROXIDE 10% W/V

K863550 · PPM

Chemistry · 20d

Cleared Feb 10, 1986

URINE DILUENT-FOR USE WITH ION SELECTIVE ELECTRODE

STAIN, METHYLENE BLUE-EOSIN

WRIGHTS STAIN SOLUTION

K843051

Pathology

Cleared May 31, 1984

CYANOMETHEMOGLOBIN REAGENT

K841799 · GIF

Hematology · 43d

Cleared May 31, 1984

LYSING & HEMOGLOBIN REAGENT

K841800 · GGK

Hematology · 43d

Cleared May 22, 1984

SCOTTS TAP WATER SUBSTITUTE 7

K841423 · JCC

Pathology · 47d

Reagent Laboratory, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Reagent Laboratory, Inc.

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