ELECTROCARDIOGRAPH (ECG) ELECTRODE, NON-STERILE— 510(k) K020003

Substantially Equivalent

Bio Protech, Inc.

FDA 510(k) clearance K020003 for ELECTROCARDIOGRAPH (ECG) ELECTRODE, NON-STERILE, Substantially Equivalent on 2002-11-07. Applicant: Bio Protech, Inc..

Clearance details

Applicant: Bio Protech, Inc.
Product code: Code DRX
Advisory panel: Cardiovascular
Date received: 2002-01-02
Decision date: 2002-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparks, NV, US

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Adverse events under product code DRX

product code DRX

Death: 6
Injury: 476
Other: 2
Total: 484

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.