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FDA 510(k)

TECHNICON H*1 SYSTEM

K-Number: K852787 · 1985-07-23

ApplicantTechnicon Instruments Corp.
Decision Date1985-07-23
Product Code
DecisionSubstantially Equivalent

Device Summary

TECHNICON H*1 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 1985-07-23 under 510(k) number K852787. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON H*1 SYSTEM?

TECHNICON H*1 SYSTEM is a medical device that received FDA 510(k) clearance on 1985-07-23. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K852787.

When did TECHNICON H*1 SYSTEM receive FDA 510(k) clearance?

TECHNICON H*1 SYSTEM received FDA 510(k) clearance on 1985-07-23, under 510(k) number K852787.

Who is the listed applicant for TECHNICON H*1 SYSTEM?

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

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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