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FDA 510(k)

URIC ACID TEST KIT

K-Number: K901001 · 1990-05-23

ApplicantElite Technology, Inc.
Decision Date1990-05-23
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Elite Technology, Inc.. It received FDA 510(k) clearance on 1990-05-23 under 510(k) number K901001. 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 KIT?

URIC ACID TEST KIT is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Elite Technology, Inc.. The 510(k) number is K901001.

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

URIC ACID TEST KIT received FDA 510(k) clearance on 1990-05-23, under 510(k) number K901001.

Who is the listed applicant for URIC ACID TEST KIT?

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

What is the FDA product code for URIC ACID TEST KIT?

The FDA product code for URIC ACID TEST KIT is KNK.

Other records listing Elite Technology, 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.

K900733PROTEIN TEST FOR URINE AND CSFK901090ELITECH GAMMA GT TEST KITK895951CHOLESTEROL TEST KITK895952TRIGLYCERIDES TEST KIT

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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