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FDA 510(k)

TOYO JOZO URIC ACID TEST

K-Number: K842103 · 1984-08-12

ApplicantAdvocacy International, Ltd.
Decision Date1984-08-12
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOYO JOZO URIC ACID TEST is the device name listed in this FDA 510(k) record. The listed applicant is Advocacy International, Ltd.. It received FDA 510(k) clearance on 1984-08-12 under 510(k) number K842103. 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 TOYO JOZO URIC ACID TEST?

TOYO JOZO URIC ACID TEST is a medical device that received FDA 510(k) clearance on 1984-08-12. The listed applicant is Advocacy International, Ltd.. The 510(k) number is K842103.

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

TOYO JOZO URIC ACID TEST received FDA 510(k) clearance on 1984-08-12, under 510(k) number K842103.

Who is the listed applicant for TOYO JOZO URIC ACID TEST?

The FDA 510(k) record lists Advocacy International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOYO JOZO URIC ACID TEST?

The FDA product code for TOYO JOZO URIC ACID TEST is KNK.

Other records listing Advocacy International, Ltd. 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.

K874027LIPASE UV [TOYO]K873792SEPACELL R-500 AND SEPACELL R-500AK855251MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERSK855212ASAHI AM SERIES DIALYZERSK854259SEPACELL R-500 & SEPACELL R-500AK842104TOYO JOZO G-GTP TEST

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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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