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FDA 510(k)

URIC ACID MODEL 3P39

K-Number: K102568 · 2011-05-06

ApplicantAbbott Laboratories
Decision Date2011-05-06
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID MODEL 3P39 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2011-05-06 under 510(k) number K102568. 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 MODEL 3P39?

URIC ACID MODEL 3P39 is a medical device that received FDA 510(k) clearance on 2011-05-06. The listed applicant is Abbott Laboratories. The 510(k) number is K102568.

When did URIC ACID MODEL 3P39 receive FDA 510(k) clearance?

URIC ACID MODEL 3P39 received FDA 510(k) clearance on 2011-05-06, under 510(k) number K102568.

Who is the listed applicant for URIC ACID MODEL 3P39?

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

What is the FDA product code for URIC ACID MODEL 3P39?

The FDA product code for URIC ACID MODEL 3P39 is KNK.

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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.

K062862OLYMPUS 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 SaicK012038JAS URIC ACID LIQUID REAGENTJas Diagnostics, 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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