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FDA 510(k)

TECHNICON C/90 SYSTEM

K-Number: K800121 · 1980-02-05

ApplicantTechnicon Instruments Corp.
Decision Date1980-02-05
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TECHNICON C/90 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 1980-02-05 under 510(k) number K800121. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON C/90 SYSTEM?

TECHNICON C/90 SYSTEM is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K800121.

When did TECHNICON C/90 SYSTEM receive FDA 510(k) clearance?

TECHNICON C/90 SYSTEM received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800121.

Who is the listed applicant for TECHNICON C/90 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 C/90 SYSTEM?

The FDA product code for TECHNICON C/90 SYSTEM is GKZ.

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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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