Seca GmbH & Co. KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seca GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Seca GmbH & Co. KG
2 devices