IDOC UPPER ARM ATTACHED BLOOD PRESSURE AND PULSE RATE MONITOR, MODEL ID-42A/ID-43A— 510(k) K052872

Substantially Equivalent

Taidoc Technology Corporation

FDA 510(k) clearance K052872 for IDOC UPPER ARM ATTACHED BLOOD PRESSURE AND PULSE RATE MONITOR, MODEL ID-42A/ID-43A, Substantially Equivalent on 2005-11-23. Applicant: Taidoc Technology Corporation.

Clearance details

Applicant: Taidoc Technology Corporation
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2005-10-11
Decision date: 2005-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Chung, Taipei, TW

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.