Accu-Speed, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accu-Speed, Incorporated - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Accu-Speed, Incorporated has 1 FDA 510(k) cleared medical devices. Based in Groton, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Accu-Speed, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accu-Speed, Incorporated
1 devices