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FDA 510(k) Application Details - K122249
Device Classification Name
Needle, Hypodermic, Single Lumen
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510(K) Number
K122249
Device Name
Needle, Hypodermic, Single Lumen
Applicant
TERUMO (PHILIPPINES) CORPORATION
950 ELKTON BLVD
ELKTON, MD 21921 US
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Contact
PHILLIP LESTER
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Regulation Number
880.5570
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Classification Product Code
FMI
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More FDA Info for this Product Code
Date Received
07/27/2012
Decision Date
08/28/2012
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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