NEUROSENSOR— 510(k) K013930

Substantially Equivalent

Novus Monitoring, Ltd.

FDA 510(k) clearance K013930 for NEUROSENSOR, Substantially Equivalent on 2002-02-20. Applicant: Novus Monitoring, Ltd..

Clearance details

Applicant: Novus Monitoring, Ltd.
Product code: Code GWM
Advisory panel: Neurology
Date received: 2001-11-28
Decision date: 2002-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: United Kingdom, GB

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Adverse events under product code GWM

product code GWM

Death: 21
Injury: 732
Malfunction: 2,063
Other: 1
Total: 2,817

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.