Medical Device Manufacturer · US , Morris Plains , NJ

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

2 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

Aristar Inc. U.S.A. has 2 FDA 510(k) cleared medical devices. Based in Morris Plains, US.

Historical record: 2 cleared submissions from 1994 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Aristar Inc. U.S.A. Filter by specialty or product code using the sidebar.

Aristar Inc. U.S.A. 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 - Aristar Inc. U.S.A.

2 devices

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