FDA 510(k) Application Details - K062663

Device Classification Name Respirator,Surgical

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510(K) Number K062663
Device Name Respirator,Surgical
Applicant MOLDEX/METRIC, INC.
10111 WEST JEFFERSON BLVD.
CULVER CITY, CA 90232 US
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Contact WILLIAM WAWRZYNIAK
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Regulation Number 878.4040

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Classification Product Code MSH
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Date Received 09/07/2006
Decision Date 10/11/2006
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Abbreviated
Reviewed By Third Party Y
Expedited Review



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