SIEGEN NEUROSCOPE— 510(k) K843464

Substantially Equivalent

Siegen Corp.

FDA 510(k) clearance K843464 for SIEGEN NEUROSCOPE, Substantially Equivalent on 1984-11-20. Applicant: Siegen Corp..

Clearance details

Applicant: Siegen Corp.
Product code: Code GWF
Advisory panel: Neurology
Date received: 1984-09-05
Decision date: 1984-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, 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.