NEUROQ 3.6— 510(k) K130451

Substantially Equivalent

Syntermed, Inc.

FDA 510(k) clearance K130451 for NEUROQ 3.6, Substantially Equivalent on 2013-05-17. Applicant: Syntermed, Inc..

Clearance details

Applicant: Syntermed, Inc.
Product code: Code KPS
Advisory panel: Radiology
Date received: 2013-02-22
Decision date: 2013-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

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