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.

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

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