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FDA 510(k)

VICON (MODIFICATION)

K-Number: K853804 · 1985-12-27

ApplicantOxford Metrics, Inc.
Decision Date1985-12-27
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VICON (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Metrics, Inc.. It received FDA 510(k) clearance on 1985-12-27 under 510(k) number K853804. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICON (MODIFICATION)?

VICON (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1985-12-27. The listed applicant is Oxford Metrics, Inc.. The 510(k) number is K853804.

When did VICON (MODIFICATION) receive FDA 510(k) clearance?

VICON (MODIFICATION) received FDA 510(k) clearance on 1985-12-27, under 510(k) number K853804.

Who is the listed applicant for VICON (MODIFICATION)?

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

What is the FDA product code for VICON (MODIFICATION)?

The FDA product code for VICON (MODIFICATION) is IKN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Oxford Metrics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K870901MT8 BIOLOGICAL TELEMETRY SYSTEM

Related Devices (Code: IKN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

Official Source

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

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