Last synced on 25 January 2026 at 3:41 am

TauTona Pneumoperitoneum Assist Device (TPAD)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242536
510(k) Type
Traditional
Applicant
Tautona Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2024
Days to Decision
50 days
Submission Type
Summary

TauTona Pneumoperitoneum Assist Device (TPAD)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242536
510(k) Type
Traditional
Applicant
Tautona Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2024
Days to Decision
50 days
Submission Type
Summary