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FDA 510(k)

TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC

K-Number: K901693 · 1990-04-25

ApplicantTechnicon Instruments Corp.
Decision Date1990-04-25
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K901693. 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 TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC?

TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K901693.

When did TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC receive FDA 510(k) clearance?

TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC received FDA 510(k) clearance on 1990-04-25, under 510(k) number K901693.

Who is the listed applicant for TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC?

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

What is the FDA product code for TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC?

The FDA product code for TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC is KNK.

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Other records listing Technicon Instruments Corp. 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.

K914888TECHNICON CHEM 1(TM) SYST (GEN2 SYST)K914511TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOLK914025TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)K912616TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTESK912413CHEM-LINK DATA BASE MANAGERK903824DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY

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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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