ARCOLITH 3021-CARDIAC PULSE GENERATOR— 510(k) K800326

Substantially Equivalent

Arco Medical Products Co.

FDA 510(k) clearance K800326 for ARCOLITH 3021-CARDIAC PULSE GENERATOR, Substantially Equivalent on 1980-03-17. Applicant: Arco Medical Products Co..

Clearance details

Applicant: Arco Medical Products Co.
Product code: Code DXY
Advisory panel: Cardiovascular
Date received: 1980-02-12
Decision date: 1980-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DXY

product code DXY

Death: 240
Injury: 2,328
Malfunction: 2,096
Total: 4,664

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.