Medical Device Manufacturer · US , Mchenry , IL

E K Ind., Inc. - FDA 510(k) Cleared Devices

50 submissions · 49 cleared · Since 1984

Total

Cleared

Denied

E K Ind., Inc. has 49 FDA 510(k) cleared pathology devices. Based in Mchenry, US.

Historical record: 49 cleared submissions from 1984 to 1984.

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

FDA 510(k) Regulatory Record - E K Ind., Inc.

50 devices

1-12 of 50

DECOLORIZING FLUIC, ACID-ALCOHOL 3%

FORMALIN-ACETO-ALCOHOL FIXATIVE

SCOTTS TAP WATER SUBSTITUTE

K842918 · JCC

Pathology · 48d

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E K Ind., Inc. - FDA 510(k) Cleared Devices

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