ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES— 510(k) K935437

Substantially Equivalent

Arbo Medical, Inc.

FDA 510(k) clearance K935437 for ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES, Substantially Equivalent on 1995-04-06. Applicant: Arbo Medical, Inc..

Clearance details

Applicant: Arbo Medical, Inc.
Product code: Code DRX
Advisory panel: Cardiovascular
Date received: 1993-11-10
Decision date: 1995-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stratford, CT, 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.