Whirlwind Wheelchair International is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Whirlwind Wheelchair International - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Whirlwind Wheelchair International has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Whirlwind Wheelchair International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Whirlwind Wheelchair International
1 devices