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FDA 510(k) Application Details - K111924
Device Classification Name
Pump, Infusion, Insulin Bolus
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510(K) Number
K111924
Device Name
Pump, Infusion, Insulin Bolus
Applicant
CALIBRA MEDICAL, INC.
220 SAGINAW DRIVE
REDWOOD CITY, CA 94063 US
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Contact
RICHARD J MEADER
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Regulation Number
880.5725
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Classification Product Code
OPP
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More FDA Info for this Product Code
Date Received
07/06/2011
Decision Date
04/10/2012
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
FDA Source Information for K111924
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