NEURO SCAN MEDICAL SYSTEMS A4000— 510(k) K001562

Name: FDA 510(k) clearance K001562
Creator: U.S. Food and Drug Administration
Published: 2000-08-16

Substantially Equivalent

Neuro Scan Labs

FDA 510(k) clearance K001562 for NEURO SCAN MEDICAL SYSTEMS A4000, Substantially Equivalent on 2000-08-16. Applicant: Neuro Scan Labs. Device class: 2.

Clearance details

Applicant: Neuro Scan Labs
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2000-05-19
Decision date: 2000-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: El Paso, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.