FDA 510(k) Application Details - K062302

Device Classification Name Bottle, Collection, Vacuum

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510(K) Number K062302
Device Name Bottle, Collection, Vacuum
Applicant MILLICORE AB
49 PLAIN STREET
NORTH ATTLEBORO, MA 02760 US
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Contact ROSINA ROBINSON
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Regulation Number 880.6740

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Classification Product Code KDQ
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Date Received 08/08/2006
Decision Date 10/06/2006
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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