VARELISA CENTROMERE ANTIBODIES
K-Number: K944171 · 1994-12-22
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Device Summary
Frequently Asked Questions
What is the VARELISA CENTROMERE ANTIBODIES?
VARELISA CENTROMERE ANTIBODIES is a medical device that received FDA 510(k) clearance on 1994-12-22. The listed applicant is Elias U.S.A., Inc.. The 510(k) number is K944171.
When did VARELISA CENTROMERE ANTIBODIES receive FDA 510(k) clearance?
VARELISA CENTROMERE ANTIBODIES received FDA 510(k) clearance on 1994-12-22, under 510(k) number K944171.
Who is the listed applicant for VARELISA CENTROMERE ANTIBODIES?
The FDA 510(k) record lists Elias U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VARELISA CENTROMERE ANTIBODIES?
The FDA product code for VARELISA CENTROMERE ANTIBODIES 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 Elias U.S.A., 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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