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FDA 510(k)

TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES

K-Number: K892929 · 1989-07-20

ApplicantTechnicon Instruments Corp.
Decision Date1989-07-20
Product CodeCHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES 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 1989-07-20 under 510(k) number K892929. The device is classified under product code CHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES?

TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K892929.

When did TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES receive FDA 510(k) clearance?

TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES received FDA 510(k) clearance on 1989-07-20, under 510(k) number K892929.

Who is the listed applicant for TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES?

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 AXON TM SYSTEM ADDITIONAL ANALYTES?

The FDA product code for TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES is CHJ.

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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: CHJ)

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.

K010670PICCOLO CHLORIDE TEST SYSTEMAbaxis, Inc.K945408340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZERCatachem, Inc.K943006CHLORIDE QVETPrisma SystemsK934136OLYMPUS CHLORIDE REAGENT, MODIFICATIONOlympus Corp.K932528OLYMPUS CHLORID REAGENT, MODIFIEDOlympus Corp.K925338OLYMPUS CHLORIDE REAGENTOlympus Corp.

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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