Medical Device Manufacturer · US , Melrose Park , IL

Alberto-Culver USA, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Total

Cleared

Denied

Alberto-Culver USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Melrose Park, US.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Obstetrics & Gynecology.

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

Alberto-Culver USA, 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 - Alberto-Culver USA, Inc.

1 devices

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