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PADCHECK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093205
510(k) Type
Traditional
Applicant
Padtest, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2010
Days to Decision
170 days
Submission Type
Summary

PADCHECK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093205
510(k) Type
Traditional
Applicant
Padtest, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2010
Days to Decision
170 days
Submission Type
Summary