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FDA 510(k) Application Details - K063202
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
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
Other 510(k) Applications for this Contact
Regulation Number
880.5090
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Classification Product Code
KMF
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More FDA Info for this Product Code
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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