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FDA 510(k)

RDW PARAMETER FOR THE TECHNICON H6000

K-Number: K834026 · 1984-01-30

ApplicantTechnicon Instruments Corp.
Decision Date1984-01-30
Product CodeGKL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RDW PARAMETER FOR THE TECHNICON H6000 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 1984-01-30 under 510(k) number K834026. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RDW PARAMETER FOR THE TECHNICON H6000?

RDW PARAMETER FOR THE TECHNICON H6000 is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K834026.

When did RDW PARAMETER FOR THE TECHNICON H6000 receive FDA 510(k) clearance?

RDW PARAMETER FOR THE TECHNICON H6000 received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834026.

Who is the listed applicant for RDW PARAMETER FOR THE TECHNICON H6000?

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 RDW PARAMETER FOR THE TECHNICON H6000?

The FDA product code for RDW PARAMETER FOR THE TECHNICON H6000 is GKL.

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Related Devices (Code: GKL)

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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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