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FDA 510(k)

VICON

K-Number: K811172 · 1981-06-16

ApplicantOxford Medilog, Inc.
Decision Date1981-06-16
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VICON is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811172. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICON?

VICON is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K811172.

When did VICON receive FDA 510(k) clearance?

VICON received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811172.

Who is the listed applicant for VICON?

The FDA 510(k) record lists Oxford Medilog, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VICON?

The FDA product code for VICON is LXJ.

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Related Devices (Code: LXJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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