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FDA 510(k) Application Details - K092823
Device Classification Name
Warmer, Thermal, Infusion Fluid
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510(K) Number
K092823
Device Name
Warmer, Thermal, Infusion Fluid
Applicant
STERIS Corporation
5960 Heisley Road
Mentor, OH 44060 US
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Contact
ROBERT F SULLIVAN
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Regulation Number
000.0000
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Classification Product Code
LGZ
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More FDA Info for this Product Code
Date Received
09/14/2009
Decision Date
12/18/2009
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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