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FDA 510(k)

THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT

K-Number: K925194 · 1993-02-05

Decision Date1993-02-05
Product CodeJZO
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Joldon Diagnostics. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K925194. The device is classified under product code JZO. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT?

THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Joldon Diagnostics. The 510(k) number is K925194.

When did THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT receive FDA 510(k) clearance?

THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT received FDA 510(k) clearance on 1993-02-05, under 510(k) number K925194.

Who is the listed applicant for THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT?

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

What is the FDA product code for THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT?

The FDA product code for THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT is JZO.

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 Joldon Diagnostics 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.

Related Devices (Code: JZO)

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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