THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT
K-Number: K925194 · 1993-02-05
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Device Summary
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
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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