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FDA 510(k)

TECHNICON TEST POINT ASSAYED HEMATOLOGY

K-Number: K842109 · 1984-07-27

ApplicantTechnicon Instruments Corp.
Decision Date1984-07-27
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TECHNICON TEST POINT ASSAYED HEMATOLOGY 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 1984-07-27 under 510(k) number K842109. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON TEST POINT ASSAYED HEMATOLOGY?

TECHNICON TEST POINT ASSAYED HEMATOLOGY is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K842109.

When did TECHNICON TEST POINT ASSAYED HEMATOLOGY receive FDA 510(k) clearance?

TECHNICON TEST POINT ASSAYED HEMATOLOGY received FDA 510(k) clearance on 1984-07-27, under 510(k) number K842109.

Who is the listed applicant for TECHNICON TEST POINT ASSAYED HEMATOLOGY?

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 TEST POINT ASSAYED HEMATOLOGY?

The FDA product code for TECHNICON TEST POINT ASSAYED HEMATOLOGY is JPK.

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Related Devices (Code: JPK)

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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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