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FDA 510(k) Application Details - K961452
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K961452
Device Name
Bandage, Liquid
Applicant
ACME UNITED CORP.
75 KINGS HWY. CUT-OFF
FAIRFIELD, CT 06430 US
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Contact
THOMAS E FLYNN
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
04/16/1996
Decision Date
05/31/1996
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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