Aerotek is one of 403 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Aerotek - FDA 510(k) Cleared Devices
Recent clearances: FORMULA IV ELECTRIC MOBILITY VEHICLE
1
Total
1
Cleared
0
Denied
Aerotek, is a staffing and workforce solutions provider with a registered FDA facility in Renfrew, Ontario, Canada. The company operates as a recruiting and staffing agency serving industrial and skilled trades sectors across North America.
Aerotek received 1 FDA 510(k) clearance from 1 total submission in the Physical Medicine category. The clearance was granted in 1996. The company is currently inactive in FDA regulatory submissions and should be treated as a historical record.
The cleared device was the FORMULA IV ELECTRIC MOBILITY VEHICLE, a Physical Medicine device. For detailed information on device names, product codes, and clearance dates, please review the full submission record.
FDA 510(k) Regulatory Record - Aerotek
1 devices