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FERTILIGENT SLOW RELEASE IUI CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141666
510(k) Type
Traditional
Applicant
FERTILIGENT, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2015
Days to Decision
225 days
Submission Type
Summary

FERTILIGENT SLOW RELEASE IUI CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141666
510(k) Type
Traditional
Applicant
FERTILIGENT, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2015
Days to Decision
225 days
Submission Type
Summary