QUANTITATIVE NEUROQ 3.0— 510(k) K072307

Substantially Equivalent

Syntermed, Inc.

FDA 510(k) clearance K072307 for QUANTITATIVE NEUROQ 3.0, Substantially Equivalent on 2008-03-14. Applicant: Syntermed, Inc.. Device class: 2.

Clearance details

Applicant: Syntermed, Inc.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 2007-08-17
Decision date: 2008-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, 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.