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FDA 510(k)

GORDON DIAGNOSTIC SYSTEM MODEL I

K-Number: K854903 · 1986-06-02

ApplicantClinical Diagnostics, Inc.
Decision Date1986-06-02
Product CodeLQD
DecisionSubstantially Equivalent

Device Summary

GORDON DIAGNOSTIC SYSTEM MODEL I is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-06-02 under 510(k) number K854903. The device is classified under product code LQD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GORDON DIAGNOSTIC SYSTEM MODEL I?

GORDON DIAGNOSTIC SYSTEM MODEL I is a medical device that received FDA 510(k) clearance on 1986-06-02. The listed applicant is Clinical Diagnostics, Inc.. The 510(k) number is K854903.

When did GORDON DIAGNOSTIC SYSTEM MODEL I receive FDA 510(k) clearance?

GORDON DIAGNOSTIC SYSTEM MODEL I received FDA 510(k) clearance on 1986-06-02, under 510(k) number K854903.

Who is the listed applicant for GORDON DIAGNOSTIC SYSTEM MODEL I?

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

What is the FDA product code for GORDON DIAGNOSTIC SYSTEM MODEL I?

The FDA product code for GORDON DIAGNOSTIC SYSTEM MODEL I is LQD.

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Other records listing Clinical Diagnostics, 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.

K971653GLUCOCHEK POCKETLAB II BLOOD GLUCOSE SYSTEMK951457GLUCOCHEK POCKETLABK940215GLUCOCHEKK771813CENTRIFICHEM SYS 400 ANALYZERK771118CENTRIA SEPARATION COLUMNS TYPE AK771117CENTRIA CORTISOL RIA

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Related Devices (Code: LQD)

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.

K173915Test of Variables of Attention (T.O.V.A.)The Tova CompanyK170082Test of Variables of Attention (T.O.V.A.) Version 9.0The Tova CompanyK143468QbCheckQbtech ABK122149QBTESQbtech ABK040894QBTESTQbtech ABK020800OPTAX SYSTEMOptax Systems, Inc.

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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