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FDA 510(k)

SERUM, URIC ACID DETERMINATION

K-Number: K790019 · 1979-02-26

ApplicantFisher Scientific Co., LLC
Decision Date1979-02-26
Product CodeCDH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERUM, URIC ACID DETERMINATION is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K790019. The device is classified under product code CDH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERUM, URIC ACID DETERMINATION?

SERUM, URIC ACID DETERMINATION is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K790019.

When did SERUM, URIC ACID DETERMINATION receive FDA 510(k) clearance?

SERUM, URIC ACID DETERMINATION received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790019.

Who is the listed applicant for SERUM, URIC ACID DETERMINATION?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERUM, URIC ACID DETERMINATION?

The FDA product code for SERUM, URIC ACID DETERMINATION is CDH.

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Other records listing Fisher Scientific Co., LLC 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.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: CDH)

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.

K850933URIC ACIDDilab, Inc.K841067URIC ACID REAGENT SETMedical Specialties, Inc.K821213URIC ACID REAGENT SETOmega Medical ElectronicsK813076PHOSPHOTUNGSTATE REDUCTION, URIC ACIDAmerican Monitor Corp.K810088URIC ACID (TPTZ) COLORINMETRICBio-Analytics Laboratories, Inc.K800672SMAC REPLACEMENT REAGENTS/DETERM-URIC-ACDiagnostic Solutions, 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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