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FDA 510(k) Application Details - K955399
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K955399
Device Name
Bandage, Liquid
Applicant
LANGE MEDICAL PRODUCTS, INC.
1676 SOUTH WOLF RD.
WHEELING, IL 60090 US
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Contact
LEON FERN
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
11/24/1995
Decision Date
02/07/1996
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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