VIBRAMETER— 510(k) K843486

Substantially Equivalent

Somedic AB

FDA 510(k) clearance K843486 for VIBRAMETER, Substantially Equivalent on 1984-12-24. Applicant: Somedic AB. Device class: 1.

Clearance details

Applicant: Somedic AB
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1984-09-06
Decision date: 1984-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sweden, 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.