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TAMPAX SCENTED & SATIN SCENTED TAMPAX-JUNIOR, REGULAR, SUPER & SUPER PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011171
510(k) Type
Traditional
Applicant
Procter & Gamble Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2001
Days to Decision
76 days
Submission Type
Summary

TAMPAX SCENTED & SATIN SCENTED TAMPAX-JUNIOR, REGULAR, SUPER & SUPER PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011171
510(k) Type
Traditional
Applicant
Procter & Gamble Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2001
Days to Decision
76 days
Submission Type
Summary