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FDA 510(k)

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER

K-Number: K101569 · 2011-03-01

ApplicantTaidoc Technology Corporation
Decision Date2011-03-01
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2011-03-01 under 510(k) number K101569. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER?

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER is a medical device that received FDA 510(k) clearance on 2011-03-01. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K101569.

When did V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER receive FDA 510(k) clearance?

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER received FDA 510(k) clearance on 2011-03-01, under 510(k) number K101569.

Who is the listed applicant for V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER?

The FDA product code for V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER is DPS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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