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FDA 510(k)

TRACE TRANSFERRIN REAGENT

K-Number: K932713 · 1993-09-30

Decision Date1993-09-30
Product CodeDDQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TRACE TRANSFERRIN REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Trace Scientific , Ltd.. It received FDA 510(k) clearance on 1993-09-30 under 510(k) number K932713. The device is classified under product code DDQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACE TRANSFERRIN REAGENT?

TRACE TRANSFERRIN REAGENT is a medical device that received FDA 510(k) clearance on 1993-09-30. The listed applicant is Trace Scientific , Ltd.. The 510(k) number is K932713.

When did TRACE TRANSFERRIN REAGENT receive FDA 510(k) clearance?

TRACE TRANSFERRIN REAGENT received FDA 510(k) clearance on 1993-09-30, under 510(k) number K932713.

Who is the listed applicant for TRACE TRANSFERRIN REAGENT?

The FDA 510(k) record lists Trace Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRACE TRANSFERRIN REAGENT?

The FDA product code for TRACE TRANSFERRIN REAGENT is DDQ.

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 Trace Scientific , Ltd. 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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Related Devices (Code: DDQ)

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.

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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