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INTRAUTERINE INSEMINATION (IUI) CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092579
510(k) Type
Traditional
Applicant
Fertiligent, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2010
Days to Decision
228 days
Submission Type
Summary

INTRAUTERINE INSEMINATION (IUI) CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092579
510(k) Type
Traditional
Applicant
Fertiligent, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2010
Days to Decision
228 days
Submission Type
Summary