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FDA 510(k)

TECHNICON CHEM 1(TM) SYSTEM

K-Number: K874916 · 1988-03-03

ApplicantTechnicon Instruments Corp.
Decision Date1988-03-03
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TECHNICON CHEM 1(TM) SYSTEM 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 1988-03-03 under 510(k) number K874916. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON CHEM 1(TM) SYSTEM?

TECHNICON CHEM 1(TM) SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K874916.

When did TECHNICON CHEM 1(TM) SYSTEM receive FDA 510(k) clearance?

TECHNICON CHEM 1(TM) SYSTEM received FDA 510(k) clearance on 1988-03-03, under 510(k) number K874916.

Who is the listed applicant for TECHNICON CHEM 1(TM) SYSTEM?

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(TM) SYSTEM?

The FDA product code for TECHNICON CHEM 1(TM) SYSTEM is LDR.

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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: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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