Medical Device Manufacturer · US , Los Angeles , CA

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

1 submissions · 1 cleared · Since 1992

Total

Cleared

Denied

Harrier, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Physical Medicine.

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

Harrier, 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 - Harrier, Inc.

1 devices

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