FDA 510(k) Application Details - K200038

Device Classification Name Hysteroscope (And Accessories)

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510(K) Number K200038
Device Name Hysteroscope (And Accessories)
Applicant CooperSurgical, Inc.
95 Corporate Drive
Trumbull, CT 06611 US
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Contact Christine Kupchick
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Regulation Number 884.1690

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Classification Product Code HIH
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Date Received 01/08/2020
Decision Date 02/05/2020
Decision SESE - SUBST EQUIV
Classification Advisory Committee OB - Obstetrics/Gynecology
Review Advisory Committee OB - Obstetrics/Gynecology
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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