Last synced on 20 December 2024 at 11:05 pm

FemVue MINI Saline-Air Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242002
510(k) Type
Traditional
Applicant
Femasys Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2024
Days to Decision
136 days
Submission Type
Summary

FemVue MINI Saline-Air Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242002
510(k) Type
Traditional
Applicant
Femasys Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2024
Days to Decision
136 days
Submission Type
Summary