Medical Device Manufacturer · US , Mchenry , IL

Organon, Inc. - FDA 510(k) Cleared Devices

41 submissions · 41 cleared · Since 1977

Total

Cleared

Denied

Organon, Inc. has 41 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 41 cleared submissions from 1977 to 1995. Primary specialty: Chemistry.

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

Organon, 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 - Organon, Inc.

41 devices

1-12 of 41

Cleared May 26, 1995

RECONSTITUTION ACCESSOREIS

K950861 · FPK

General Hospital · 88d

OREIA II B-HCG PREGNANCY TEST KIT

K841525 · JHI

Chemistry · 54d

Cleared May 22, 1984

ACCURATE BETA 30 PREGNANCY TEST KIT

OREIA II B-HCG, ENZYME INNUNOASSAY

K832801 · JHI

Chemistry · 112d

Cleared Jun 08, 1983

NEO-PREGNOSTICON DUOCLON TUBE TEST

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Organon, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Organon, Inc.

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