Accelerated Care Plus Corp. is one of 23730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accelerated Care Plus Corp. - FDA 510(k) Cleared Devices
Recent clearances: ACP OMNIPAD LIGHT THERAPY SYSTEM & ACP OMNIPAD 500 CONTROL UNIT
1
Total
1
Cleared
0
Denied
Accelerated Care Plus Corp. has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Accelerated Care Plus Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Accelerated Care Plus Corp.
1 devices