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FDA 510(k)

URIC ACID TEST

K-Number: K811810 · 1981-07-15

ApplicantEnvironmental Chemical Specialties
Decision Date1981-07-15
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID TEST is the device name listed in this FDA 510(k) record. The listed applicant is Environmental Chemical Specialties. It received FDA 510(k) clearance on 1981-07-15 under 510(k) number K811810. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URIC ACID TEST?

URIC ACID TEST is a medical device that received FDA 510(k) clearance on 1981-07-15. The listed applicant is Environmental Chemical Specialties. The 510(k) number is K811810.

When did URIC ACID TEST receive FDA 510(k) clearance?

URIC ACID TEST received FDA 510(k) clearance on 1981-07-15, under 510(k) number K811810.

Who is the listed applicant for URIC ACID TEST?

The FDA 510(k) record lists Environmental Chemical Specialties as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIC ACID TEST?

The FDA product code for URIC ACID TEST is KNK.

Other records listing Environmental Chemical Specialties 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.

K812635ANEMIA CONTROLK811811TDM ANTI-CONVULSANT CONTROL LEVELS I-IIK811809ANTI-ARRHYTHMIC CONTROL LEVELS I & IIK803089GAMMA-GLUTAMYL TRANSPEPTIDASE (GGT)K792377CARCINOEMBRYONIC ANTIGEN (CEA) CONTROLK801854SPINAL FLUID CONTROL(HUMAN)

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Related Devices (Code: KNK)

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.

K102568URIC ACID MODEL 3P39Abbott LaboratoriesK062862OLYMPUS URIC ACID REAGENT, MODEL OSR6X98Olympus America, Inc.K040467VITALAB URIC ACID REAGENTClinical Data, Inc.K031044ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATORClinical Data, Inc.K022096URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEMBayer Diagnostics Corp.K023550WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDAWiener Laboratories Saic

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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