NEUROPROBES— 510(k) K052527

Substantially Equivalent

Alpha Omega Engineering , Ltd.

FDA 510(k) clearance K052527 for NEUROPROBES, Substantially Equivalent on 2006-04-12. Applicant: Alpha Omega Engineering , Ltd.. Device class: 2.

Clearance details

Applicant: Alpha Omega Engineering , Ltd.
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 2005-09-12
Decision date: 2006-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nazareth Illit, IL

Download summary PDF View on FDA.gov ↗

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