NEUROMETER— 510(k) K853608

Substantially Equivalent

Neurotron, Inc.

FDA 510(k) clearance K853608 for NEUROMETER, Substantially Equivalent on 1986-06-12. Applicant: Neurotron, Inc.. Device class: 1.

Clearance details

Applicant: Neurotron, Inc.
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1985-08-28
Decision date: 1986-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baltimore, MD, 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.