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FEMTEN CERVICAL TENACULUM

Page Type
Cleared 510(K)
510(k) Number
K062563
510(k) Type
Traditional
Applicant
Fem Suite, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2007
Days to Decision
260 days
Submission Type
Summary

FEMTEN CERVICAL TENACULUM

Page Type
Cleared 510(K)
510(k) Number
K062563
510(k) Type
Traditional
Applicant
Fem Suite, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2007
Days to Decision
260 days
Submission Type
Summary