Track Corporation is one of 25091 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Track Corporation - FDA 510(k) Cleared Devices
Recent clearances: K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT
1
Total
1
Cleared
0
Denied
Track Corporation has 1 FDA 510(k) cleared medical devices. Based in Spring Lake, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Track Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Track Corporation
1 devices