NEURONET— 510(k) K952294

Substantially Equivalent

Computational Diagnostics, Inc.

FDA 510(k) clearance K952294 for NEURONET, Substantially Equivalent on 1996-01-26. Applicant: Computational Diagnostics, Inc..

Clearance details

Applicant: Computational Diagnostics, Inc.
Product code: Code GWF
Advisory panel: Neurology
Date received: 1995-05-16
Decision date: 1996-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GWF

product code GWF

Malfunction: 2,364
Other: 4
Total: 2,368

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.