FDA 510(k) Application Details - K152904

Device Classification Name Media, Reproductive

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510(K) Number K152904
Device Name Media, Reproductive
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 884.6180

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Classification Product Code MQL
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Date Received 10/01/2015
Decision Date 12/03/2015
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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