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FDA 510(k) Application Details - K092712
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K092712
Device Name
Bandage, Liquid
Applicant
LODESTAR PRODUCTS, INC.
6833 SAINT LAWRENCE ST.
PLANO, TX 75024 US
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ERIC LUO
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
09/03/2009
Decision Date
02/23/2010
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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