DIGITAL ELECTRONEUROMETER S-100— 510(k) K843924

Name: FDA 510(k) clearance K843924
Creator: U.S. Food and Drug Administration
Published: 1985-03-12

Substantially Equivalent

Neurotron, Inc.

FDA 510(k) clearance K843924 for DIGITAL ELECTRONEUROMETER S-100, Substantially Equivalent on 1985-03-12. Applicant: Neurotron, Inc.. Device class: 2.

Clearance details

Applicant: Neurotron, Inc.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 1984-10-05
Decision date: 1985-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lawrenceville, NJ, US

Download summary PDF View on FDA.gov ↗

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