THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE
K-Number: K024031 · 2003-02-06
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Device Summary
Frequently Asked Questions
What is the THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE?
THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE is a medical device that received FDA 510(k) clearance on 2003-02-06. The listed applicant is Theratest Laboratories, Inc.. The 510(k) number is K024031.
When did THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE receive FDA 510(k) clearance?
THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE received FDA 510(k) clearance on 2003-02-06, under 510(k) number K024031.
Who is the listed applicant for THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE?
The FDA 510(k) record lists Theratest Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE?
The FDA product code for THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE is LJM.
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 Theratest Laboratories, Inc. 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: LJM)
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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