Gc Medtech, LLC is one of 18890 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gc Medtech, LLC - FDA 510(k) Cleared Devices
Recent clearances: E-App, GENTLECARE AR APPLICATOR
2
Total
2
Cleared
0
Denied
Gc Medtech, LLC has 2 FDA 510(k) cleared medical devices. Based in Lutsen, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Gc Medtech, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Strategies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Gc Medtech, LLC
2 devices