Kingyield Wrist Blood Pressure Monitor

FDA 510(k) K112042 · Shenzhen Kingyield Technology Co., Ltd.

Substantially Equivalent

510(k) numberK112042

Submission

Device name
Kingyield Wrist Blood Pressure Monitor
Applicant
Shenzhen Kingyield Technology Co., Ltd.
Shenzhen, Guangdong, CN
Received
July 18, 2011
Decision date
February 10, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
DXN – System, Measurement, Blood-Pressure, Non-Invasive
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1130
Specialty
Cardiovascular

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More from 80 Beats Medical GmbH

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Questions and answers

When was Kingyield Wrist Blood Pressure Monitor cleared by the FDA?

Kingyield Wrist Blood Pressure Monitor (K112042) received a 510(k) decision of Substantially Equivalent on February 10, 2012, 207 days after the submission was received.

What is the product code of K112042?

The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.