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U.S. Department of Health and Human Services

Product Classification
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Device cannula, intrauterine insemination
Regulation Description Cervical cap.
Regulation Medical Specialty Obstetrics/Gynecology
Review Panel Obstetrics/Gynecology
Product CodeMFD
Submission Type 510(k)
Regulation Number 884.5250
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review Not Third Party Eligible
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