V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER— 510(k) K101569

Substantially Equivalent

Taidoc Technology Corporation

FDA 510(k) clearance K101569 for V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER, Substantially Equivalent on 2011-03-01. Applicant: Taidoc Technology Corporation.

Clearance details

Applicant: Taidoc Technology Corporation
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 2010-06-04
Decision date: 2011-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei County, TW

Download summary PDF View on FDA.gov ↗

Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.