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FDA 510(k) Application Details - K955453
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K955453
Device Name
Bandage, Liquid
Applicant
WESTAIM TECHNOLOGIES, INC.
555 13TH STREET, N.W.
WASHINGTON, DC 20004-1109 US
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Contact
JONATHAN S KAHAN
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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
11/29/1995
Decision Date
05/31/1996
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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