Last synced on 25 January 2026 at 3:41 am

FEMVUE(TM) CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083690
510(k) Type
Traditional
Applicant
Femasys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2009
Days to Decision
193 days
Submission Type
Summary

FEMVUE(TM) CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083690
510(k) Type
Traditional
Applicant
Femasys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2009
Days to Decision
193 days
Submission Type
Summary