Accelerated Care Plus is one of 4783 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accelerated Care Plus - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Accelerated Care Plus has 2 FDA 510(k) cleared medical devices. Based in Reno, US.
Historical record: 2 cleared submissions from 2009 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Accelerated Care Plus Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accelerated Care Plus
2 devices