Fast Track Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fast Track Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iRelieve Microcurrent Pain Relief System
1
Total
1
Cleared
0
Denied
Fast Track Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fast Track Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Affairs Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Fast Track Technologies, Inc.
1 devices