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Milli Vaginal Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211959
510(k) Type
Traditional
Applicant
Materna Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2021
Days to Decision
160 days
Submission Type
Summary

Milli Vaginal Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211959
510(k) Type
Traditional
Applicant
Materna Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2021
Days to Decision
160 days
Submission Type
Summary