Medical Device Manufacturer · US , Washington , DC

Seca GmbH & Co. KG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Seca GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 2013 to 2020. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Seca GmbH & Co. KG Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Seca GmbH & Co. KG

2 devices

1-2 of 2