Geomed Medizin-Technik GmbH & Co. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Geomed Medizin-Technik GmbH & Co. - FDA 510(k) Cleared Devices
Recent clearances: Geomed Vascular Dilators
2
Total
2
Cleared
0
Denied
Geomed Medizin-Technik GmbH & Co. has 2 FDA 510(k) cleared medical devices. Based in Amsterdam, Nh, NL.
Historical record: 2 cleared submissions from 2005 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Geomed Medizin-Technik GmbH & Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Business Support International as regulatory consultant.
FDA 510(k) Regulatory Record - Geomed Medizin-Technik GmbH & Co.
2 devices