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FDA 510(k) Application Details - K110723
Device Classification Name
Oximeter, Reprocessed
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510(K) Number
K110723
Device Name
Oximeter, Reprocessed
Applicant
MASIMO CORPORATION
40 PARKER
IRVINE, CA 92618 US
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Contact
SHELLY HARRIS
Other 510(k) Applications for this Contact
Regulation Number
870.2700
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Classification Product Code
NLF
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More FDA Info for this Product Code
Date Received
03/16/2011
Decision Date
07/28/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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