BZ-576 NON-INVASIVE AUTOMATIC BLOOD PRESSURE MONITOR— 510(k) K033216

Substantially Equivalent

The Buzz Group, LLC

FDA 510(k) clearance K033216 for BZ-576 NON-INVASIVE AUTOMATIC BLOOD PRESSURE MONITOR, Substantially Equivalent on 2004-05-04. Applicant: The Buzz Group, LLC.

Clearance details

Applicant: The Buzz Group, LLC
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2003-10-03
Decision date: 2004-05-04
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Deer Field, IL, US

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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.