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FDA 510(k)

CARESIDE URIC ACID

K-Number: K981604 · 1998-06-25

ApplicantCareside, Inc.
Decision Date1998-06-25
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARESIDE URIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Careside, Inc.. It received FDA 510(k) clearance on 1998-06-25 under 510(k) number K981604. 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 CARESIDE URIC ACID?

CARESIDE URIC ACID is a medical device that received FDA 510(k) clearance on 1998-06-25. The listed applicant is Careside, Inc.. The 510(k) number is K981604.

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

CARESIDE URIC ACID received FDA 510(k) clearance on 1998-06-25, under 510(k) number K981604.

Who is the listed applicant for CARESIDE URIC ACID?

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

What is the FDA product code for CARESIDE URIC ACID?

The FDA product code for CARESIDE URIC ACID is KNK.

Related Clinical Trials

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Other records listing Careside, 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.

K020484CARESIDE LDHK020486CARESIDE GGTK020487CARESIDE ALTK020488CARESIDE TRGLYCERIDEK002792CARESIDE CHOLINESTERASEK001462CARESIDE HEMOGLOBIN

View all 22 devices →

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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