Medical Device Manufacturer · US , Redwood City , CA

Tautona Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tautona Group Obstetrics & Gynecology ✕
1 devices
1-1 of 1
Cleared CT Oct 15, 2024
TauTona Pneumoperitoneum Assist Device (TPAD)
K242536 · HIF
Obstetrics & Gynecology · 50d
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