Medical Device Manufacturer · US , Washington , DC

Chempaq A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Chempaq A/S has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 2005 to 2009. Primary specialty: Hematology.

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

Chempaq A/S 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 - Chempaq A/S

2 devices

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