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. Device class: 2.

Clearance details

Applicant
Taidoc Technology Corporation
Product code
Code DXN
Device class
Class 2
Regulation
21 CFR 870.1130
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Chung, Taipei, TW
Download summary PDFView on FDA.gov ↗

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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, through . 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.