PREGELLED DISPOSABLE EELCTRO. SERIES 600— 510(k) K791140

Substantially Equivalent

Hayes Products, Inc.

FDA 510(k) clearance K791140 for PREGELLED DISPOSABLE EELCTRO. SERIES 600, Substantially Equivalent on 1979-07-10. Applicant: Hayes Products, Inc..

Clearance details

Applicant: Hayes Products, Inc.
Product code: Code DRX
Advisory panel: Cardiovascular
Date received: 1979-06-18
Decision date: 1979-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.