Medical Device Manufacturer · US , Osceola , WI

Elias U.S.A., Inc. - FDA 510(k) Cleared Devices

54 submissions · 54 cleared · Since 1992

Total

Cleared

Denied

Elias U.S.A., Inc. has 54 FDA 510(k) cleared immunology devices. Based in Osceola, US.

Historical record: 54 cleared submissions from 1992 to 1997.

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

Elias U.S.A., 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 - Elias U.S.A., Inc.

54 devices

1-12 of 54

VARELISA ANA (4) PROFILE

K963291 · LJM

Immunology · 40d

Cleared Aug 30, 1996

VARELISA HELICOBACTER PYLORI ANTIBODIES

VARELISA CARDIOLIPIN ABS SCREEN

K951187 · MID

Immunology · 200d

Cleared Apr 17, 1995

VARELISA COMBINED DNA ANTIBODIES EIA

K944334 · LRM

Immunology · 223d

Cleared Apr 17, 1995

VARELISA ANA-4 SCREEN

VARELISA PARIETAL CELL ANTIBODIES

K951206 · MLE

Immunology · 31d

Cleared Apr 17, 1995

VARELISA HISTONE ANTIBODIES

K951207 · LJM

Immunology · 31d

Cleared Mar 10, 1995

VARELISA DSDNA ANTIBODIES (FARR VERSION)

K950031 · LRM

Immunology · 65d

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Elias U.S.A., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Elias U.S.A., Inc.

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