FDA 510(k) Application Details - K173431

Device Classification Name Catheter, Assisted Reproduction

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510(K) Number K173431
Device Name Catheter, Assisted Reproduction
Applicant William A. Cook Australia PTY LTD
95 Brandl Street
Eight Mile Plains 4113 AU
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Contact Gordana Pozvek
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Regulation Number 884.6110

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Classification Product Code MQF
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Date Received 11/02/2017
Decision Date 05/18/2018
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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