Medical Device Manufacturer · US , Roselle , IL

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

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Arjo, Inc. has 1 FDA 510(k) cleared medical devices. Based in Roselle, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Physical Medicine.

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

Arjo, 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 - Arjo, Inc.

1 devices

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