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FDA 510(k) Application Details - K973429
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K973429
Device Name
Bandage, Liquid
Applicant
BIODERM, INC.
25 WEST 752 WHITE BIRCH LN.
WHEATON, IL 60187 US
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Contact
GEORGE WORTHLEY
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
09/10/1997
Decision Date
12/01/1997
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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