SunTech CT40 Spot-check Vital Signs Device

FDA 510(k) K160439 · Suntech Medical

Substantially Equivalent

510(k) numberK160439

Submission

Device name
SunTech CT40 Spot-check Vital Signs Device
Applicant
Suntech Medical
Morrisville, NC, US
Received
February 17, 2016
Decision date
July 6, 2016
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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 SunTech CT40 Spot-check Vital Signs Device cleared by the FDA?

SunTech CT40 Spot-check Vital Signs Device (K160439) received a 510(k) decision of Substantially Equivalent on July 6, 2016, 140 days after the submission was received.

What is the product code of K160439?

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