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

Fully Automatic Electronic Blood Pressure Monitor

K Number: K162230 · Decision Nov 18, 2016
Classifications
1
FEI Numbers
420
Registration Numbers
420
Same Product Code
1186
Applicant Total
1
Review Days
102

Basic Information

Device Name
Fully Automatic Electronic Blood Pressure Monitor
K Number
K162230
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ADON HEALTH CO., LTD.
Date Received
August 8, 2016
Decision Date
November 18, 2016
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

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