Turbo Wheelchair Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Turbo Wheelchair Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: Merlexi Craft Bariatric series of manual wheelchairs
2
Total
2
Cleared
0
Denied
Turbo Wheelchair Co., Inc. has 2 FDA 510(k) cleared medical devices. Based in Beaufort, US.
Latest FDA clearance: Jul 2024. Active since 2003. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Turbo Wheelchair Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Turbo Wheelchair Co., Inc.
2 devices