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FEMVUE CORNUAL BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K100662
510(k) Type
Special
Applicant
FEMASYS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2010
Days to Decision
30 days
Submission Type
Summary

FEMVUE CORNUAL BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K100662
510(k) Type
Special
Applicant
FEMASYS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2010
Days to Decision
30 days
Submission Type
Summary