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FEMVUE(TM) CATHETER SYSTEM

Page Type
Cleared 510(K)
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)
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