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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Hypodermic, Single Lumen
510(k) Number K150263
Device Name K-Pack II Needle-21G x 2
Applicant
Terumo Europe N.V.
Interleuvenlaan 40
Leuven,  BE 3001
Applicant Contact M J Aerts
Correspondent
Terumo Europe N.V.
Interleuvenlaan 40
Leuven,  BE 3001
Correspondent Contact M J Aerts
Regulation Number880.5570
Classification Product Code
FMI  
Date Received02/04/2015
Decision Date 04/01/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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