Medical Device Manufacturer · US , Washington, Dc , DC

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

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Escreen, Inc. has 1 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Toxicology.

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

Escreen, 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 - Escreen, Inc.

1 devices

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