Canady Technology, LLC is one of 25351 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Canady Technology, LLC - FDA 510(k) Cleared Devices
Recent clearances: CANADY PLASMA PROBES
1
Total
1
Cleared
0
Denied
Canady Technology, LLC has 1 FDA 510(k) cleared medical devices. Based in Hampton, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Canady Technology, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Canady Technology, LLC
1 devices