The Gotzen Group, Inc. is one of 25917 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Gotzen Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DEGOTZEN SYNCHRO
1
Total
1
Cleared
0
Denied
The Gotzen Group, Inc. has 1 FDA 510(k) cleared medical devices. Based in Flanders, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by The Gotzen Group, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - The Gotzen Group, Inc.
1 devices