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.

E K Ind., 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 - 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

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

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