Electronic Sphygmomanometer

FDA 510(k) K110774 · Contec Medical System Co., Ltd.

Substantially Equivalent

510(k) numberK110774

Submission

Device name
Electronic Sphygmomanometer
Applicant
Contec Medical System Co., Ltd.
Shanghai, CN
Received
March 21, 2011
Decision date
May 13, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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Questions and answers

When was Electronic Sphygmomanometer cleared by the FDA?

Electronic Sphygmomanometer (K110774) received a 510(k) decision of Substantially Equivalent on May 13, 2011, 53 days after the submission was received.

What is the product code of K110774?

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