Medical Device Manufacturer · US , Lanham , MD

Ancie Laboratories - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

Total

Cleared

Denied

Ancie Laboratories has 1 FDA 510(k) cleared medical devices. Based in Lanham, US.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Ophthalmic.

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

Ancie 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 - Ancie Laboratories

1 devices

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