Last synced on 14 November 2025 at 11:06 pm

TheyFit Male Condom

Page Type
Cleared 510(K)
510(k) Number
K150072
510(k) Type
Traditional
Applicant
THEYFIT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2015
Days to Decision
90 days
Submission Type
Summary

TheyFit Male Condom

Page Type
Cleared 510(K)
510(k) Number
K150072
510(k) Type
Traditional
Applicant
THEYFIT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2015
Days to Decision
90 days
Submission Type
Summary