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FDA 510(k) Application Details - K954728
Device Classification Name
Bandage, Liquid
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510(K) Number
K954728
Device Name
Bandage, Liquid
Applicant
CONTINENTAL MEDICAL LABORATORIES, INC.
P.O. BOX 306
817 MOHR AVENUE
WATERFORD, WI 53185 US
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Contact
JOSEPH DUNN
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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
10/13/1995
Decision Date
09/23/1996
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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