NUAMPS— 510(k) K023536

Name: FDA 510(k) clearance K023536
Creator: U.S. Food and Drug Administration
Published: 2003-01-15

Substantially Equivalent

Neuroscan

FDA 510(k) clearance K023536 for NUAMPS, Substantially Equivalent on 2003-01-15. Applicant: Neuroscan. Device class: 2.

Clearance details

Applicant: Neuroscan
Product code: Code OLT
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2002-10-21
Decision date: 2003-01-15
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: El Paso, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code OLT

product code OLT

Other: 1
Total: 1

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.