Vtrust Blood Pressure Monitor, Model Vtrust 701DH

FDA 510(k) K091414 · Biocare Corp.

Substantially Equivalent

510(k) numberK091414

Submission

Device name
Vtrust Blood Pressure Monitor, Model Vtrust 701DH
Applicant
Biocare Corp.
Taoyuan, TW
Received
May 13, 2009
Decision date
October 21, 2009
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 Vtrust Blood Pressure Monitor, Model Vtrust 701DH cleared by the FDA?

Vtrust Blood Pressure Monitor, Model Vtrust 701DH (K091414) received a 510(k) decision of Substantially Equivalent on October 21, 2009, 161 days after the submission was received.

What is the product code of K091414?

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