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TauTona Pneumoperitoneum Assist Device (TPAD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233020
510(k) Type
Traditional
Applicant
TauTona Group Research & Development, Co. LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
112 days
Submission Type
Summary

TauTona Pneumoperitoneum Assist Device (TPAD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233020
510(k) Type
Traditional
Applicant
TauTona Group Research & Development, Co. LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
112 days
Submission Type
Summary