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FDA 510(k) Application Details - K124026
Device Classification Name
Introducer, Syringe Needle
More FDA Info for this Device
510(K) Number
K124026
Device Name
Introducer, Syringe Needle
Applicant
SCANDINAVIAN HEALTH LIMITED
#588 JIM MORAN BLVD
DEERFIELD BEACH, FL 33442 US
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Contact
James Haynes
Other 510(k) Applications for this Contact
Regulation Number
880.6920
More FDA Info for this Regulation Number
Classification Product Code
KZH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/28/2012
Decision Date
09/13/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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