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FEMECC ENDOCERVICAL CURETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060320
510(k) Type
Traditional
Applicant
FEMSPEC L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2006
Days to Decision
170 days
Submission Type
Summary

FEMECC ENDOCERVICAL CURETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060320
510(k) Type
Traditional
Applicant
FEMSPEC L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2006
Days to Decision
170 days
Submission Type
Summary