TauTona Pneumoperitoneum Assist Device (TPAD)
Oct 2024
50d
Tautona Group
1
Total
1
Cleared
0
Denied
Tautona Group — FDA 510(k) Submissions
Tautona Group has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Insufflator, Laparoscopic . Use the specialty filter in the sidebar to narrow results.
1 devices