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FDA 510(k)

MODIFIED PARAMAX URIC ACID REAGENT

K-Number: K896521 · 1990-02-16

ApplicantBaxter Healthcare Corp
Decision Date1990-02-16
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODIFIED PARAMAX URIC ACID REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1990-02-16 under 510(k) number K896521. 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 MODIFIED PARAMAX URIC ACID REAGENT?

MODIFIED PARAMAX URIC ACID REAGENT is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K896521.

When did MODIFIED PARAMAX URIC ACID REAGENT receive FDA 510(k) clearance?

MODIFIED PARAMAX URIC ACID REAGENT received FDA 510(k) clearance on 1990-02-16, under 510(k) number K896521.

Who is the listed applicant for MODIFIED PARAMAX URIC ACID REAGENT?

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

What is the FDA product code for MODIFIED PARAMAX URIC ACID REAGENT?

The FDA product code for MODIFIED PARAMAX URIC ACID REAGENT is KNK.

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Other records listing Baxter Healthcare Corp as applicant

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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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