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FDA 510(k) Application Details - K173024
Device Classification Name
System, Measurement, Blood-Pressure, Non-Invasive
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510(K) Number
K173024
Device Name
System, Measurement, Blood-Pressure, Non-Invasive
Applicant
Joytech Healthcare Co.,Ltd
No. 365 Wuzhou Road, Yuhang Economic Development Zone
Hangzhou 311100 CN
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Contact
Ren Yunhua
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Regulation Number
870.1130
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Classification Product Code
DXN
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More FDA Info for this Product Code
Date Received
09/28/2017
Decision Date
08/22/2018
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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