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MILEX CONTRACEPTIVE DIAPHRAGM, OMNIFLEX DIAPHRAGMS, ARCING DIAPHRAGMS, WIDESEAL DIAPHRAGMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063223
510(k) Type
Traditional
Applicant
COOPERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2008
Days to Decision
456 days
Submission Type
Summary

MILEX CONTRACEPTIVE DIAPHRAGM, OMNIFLEX DIAPHRAGMS, ARCING DIAPHRAGMS, WIDESEAL DIAPHRAGMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063223
510(k) Type
Traditional
Applicant
COOPERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2008
Days to Decision
456 days
Submission Type
Summary