DERMATRON SKIN RESISTANCE METER— 510(k) K883112

Name: FDA 510(k) clearance K883112
Creator: U.S. Food and Drug Administration
Published: 1989-08-10

Substantially Equivalent

Raymar Electronics

FDA 510(k) clearance K883112 for DERMATRON SKIN RESISTANCE METER, Substantially Equivalent on 1989-08-10. Applicant: Raymar Electronics. Device class: 2.

Clearance details

Applicant: Raymar Electronics
Product code: Code GZO
Device class: Class 2
Regulation: 21 CFR 882.1540
Advisory panel: Neurology
Date received: 1988-07-25
Decision date: 1989-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oxon Rg9 1ll, England, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.