CARDIODAY, VERSION 2.0— 510(k) K070280

Substantially Equivalent

Getemed Medizin- Und Informationstechnik AG

FDA 510(k) clearance K070280 for CARDIODAY, VERSION 2.0, Substantially Equivalent on 2007-02-23. Applicant: Getemed Medizin- Und Informationstechnik AG.

Clearance details

Applicant: Getemed Medizin- Und Informationstechnik AG
Product code: Code DQK
Advisory panel: Cardiovascular
Date received: 2007-01-29
Decision date: 2007-02-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

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.