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FDA 510(k)

TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL

K-Number: K834603 · 1984-01-30

Decision Date1984-01-30
Product Code
DecisionSubstantially Equivalent

Device Summary

TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL 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 K834603. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL?

TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL 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 K834603.

When did TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL receive FDA 510(k) clearance?

TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834603.

Who is the listed applicant for TRANSFERRIN, ANTIGEN, ANTIBODY, CONTROL?

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

Related Clinical Trials

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.

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.

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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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