Medical Device Manufacturer · US , Los Angeles , CA

Line One Laboratories - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1997

Total

Cleared

Denied

Line One Laboratories has 5 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 5 cleared submissions from 1997 to 1999. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Line One Laboratories Filter by specialty or product code using the sidebar.

Line One Laboratories 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 - Line One Laboratories

5 devices

1-5 of 5