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FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122658
510(k) Type
Traditional
Applicant
FEMASYS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2012
Days to Decision
111 days
Submission Type
Summary

FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122658
510(k) Type
Traditional
Applicant
FEMASYS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2012
Days to Decision
111 days
Submission Type
Summary