Tango M2 Blood Pressure Monitor

FDA 510(k) K122401 · Suntech Medical, Inc.

Substantially Equivalent

510(k) numberK122401

Submission

Device name
Tango M2 Blood Pressure Monitor
Applicant
Suntech Medical, Inc.
Morrisville, NC, US
Received
August 7, 2012
Decision date
November 2, 2012
Decision
Substantially Equivalent (SESE)
Type
Special 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 Tango M2 Blood Pressure Monitor cleared by the FDA?

Tango M2 Blood Pressure Monitor (K122401) received a 510(k) decision of Substantially Equivalent on November 2, 2012, 87 days after the submission was received.

What is the product code of K122401?

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