Tristan Technologies, Inc. is one of 18390 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tristan Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MagView BIOMAGNETOMETER SYSTEM, MODEL 621/624 BIOMAGNETOMETER, BABYMEG BIOMAGNETOMETER SYSTEM
3
Total
3
Cleared
0
Denied
Tristan Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Encinitas, US.
Historical record: 3 cleared submissions from 2014 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Tristan Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eugene Hirschkoff, Consultant as regulatory consultant.
FDA 510(k) Regulatory Record - Tristan Technologies, Inc.
3 devices