PRESSON ELECTRODE— 510(k) K103103

Substantially Equivalent

Persyst Development Corp.

FDA 510(k) clearance K103103 for PRESSON ELECTRODE, Substantially Equivalent on 2011-12-08. Applicant: Persyst Development Corp.. Device class: 2.

Clearance details

Applicant: Persyst Development Corp.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 2010-10-20
Decision date: 2011-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Prescott, AZ, 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.