Thoracent, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Thoracent, Inc. has 1 FDA 510(k) cleared medical devices. Based in Huntington, US.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Thoracent, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Thoracent, Inc.
1 devices