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FDA 510(k) Application Details - K071384
Device Classification Name
System, Measurement, Blood-Pressure, Non-Invasive
More FDA Info for this Device
510(K) Number
K071384
Device Name
System, Measurement, Blood-Pressure, Non-Invasive
Applicant
NIHON SEIMITSU SOKKI CO., LTD.
3F, 2-17-6 AKEBONO-CHO
TACHIKAWA- SHI 190-0012 JP
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Contact
KOJI KUBO
Other 510(k) Applications for this Contact
Regulation Number
870.1130
More FDA Info for this Regulation Number
Classification Product Code
DXN
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More FDA Info for this Product Code
Date Received
05/17/2007
Decision Date
10/09/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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