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FDA 510(k)

URIC ACID KIT

K-Number: K792545 · 1980-01-29

ApplicantAlta Diagnostics, Inc.
Decision Date1980-01-29
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Alta Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K792545. 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 KIT?

URIC ACID KIT is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Alta Diagnostics, Inc.. The 510(k) number is K792545.

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

URIC ACID KIT received FDA 510(k) clearance on 1980-01-29, under 510(k) number K792545.

Who is the listed applicant for URIC ACID KIT?

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

What is the FDA product code for URIC ACID KIT?

The FDA product code for URIC ACID KIT is KNK.

Other records listing Alta 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.

K800327MAGNESIUM REAGENTK792546FETAL CHECKK790797AMYLASE REAGENT SETK790796LIPASE REAGENT SET

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

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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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