FDA 510(k) Application Details - K063202

Device Classification Name Bandage, Liquid

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510(K) Number K063202
Device Name Bandage, Liquid
Applicant PROCUREMENT TECHNOLOGY SYSTEMS, LLC
2375 HIGHWAY 101 SOUTH
BLDG A
GREER, SC 29651 US
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Contact WILLIAM J GRISWOLD
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Regulation Number 880.5090

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Classification Product Code KMF
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Date Received 10/20/2006
Decision Date 05/02/2007
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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