Arch Catheter, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arch Catheter, LLC - FDA 510(k) Cleared Devices
Recent clearances: Gatekeeper Balloon Catheter
1
Total
1
Cleared
0
Denied
Arch Catheter, LLC has 1 FDA 510(k) cleared medical devices. Based in Ninety Six, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arch Catheter, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy as regulatory consultant.
FDA 510(k) Regulatory Record - Arch Catheter, LLC
1 devices