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FDA 510(k) Application Details - K991608
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K991608
Device Name
Bandage, Liquid
Applicant
DERMAPHYLYX, INC.
12106, WEST 75TH LN.
ARVADA, CO 80005-5306 US
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Contact
ANDREW M REED
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
05/10/1999
Decision Date
07/20/1999
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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