VICON— 510(k) K811172

Substantially Equivalent

Oxford Medilog, Inc.

FDA 510(k) clearance K811172 for VICON, Substantially Equivalent on 1981-06-16. Applicant: Oxford Medilog, Inc.. Device class: 2.

Clearance details

Applicant: Oxford Medilog, Inc.
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 1981-04-28
Decision date: 1981-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.