TauTona Pneumoperitoneum Assist Device (TPAD)
Jan 2024
112d
Tautona Group Research & Development, Co., LLC - FDA 510(k) Cleared D...
1
Total
1
Cleared
0
Denied
Tautona Group Research & Development, Co., LLC has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Tautona Group Research & Development, Co., LLC Filter by specialty or product code using the sidebar.
1 devices