Aqure Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aqure Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Anchor Dual Lumen Guidewire Catheter
1
Total
1
Cleared
0
Denied
Aqure Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rogers, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Aqure Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aqure Medical, Inc.
1 devices