FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Arm Blood Pressure Monitor

K Number: K183491 · Decision Mar 24, 2019
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
6
Review Days
97

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Basic Information

Device Name
Arm Blood Pressure Monitor
K Number
K183491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xuzhou Yongkang Electronic Science Technology Co., Ltd.
Date Received
December 17, 2018
Decision Date
March 24, 2019
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

Similar 510(k) Clearances

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Other Clearances by Xuzhou Yongkang Electronic Science Technology Co., Ltd.

K Number Device Name
K252709 Wireless Probe Type Ultrasound Scanner
K191571 UV Radiation Treatment System
K180314 Infrared Thermometer
K162616 Wrist Type Blood Pressure Monitor
K161938 Fingertip Pulse Oximeter