VARELISA LA (SS-B) ANTIBODIES
K-Number: K944168 · 1994-12-22
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Device Summary
Frequently Asked Questions
What is the VARELISA LA (SS-B) ANTIBODIES?
VARELISA LA (SS-B) 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 K944168.
When did VARELISA LA (SS-B) ANTIBODIES receive FDA 510(k) clearance?
VARELISA LA (SS-B) ANTIBODIES received FDA 510(k) clearance on 1994-12-22, under 510(k) number K944168.
Who is the listed applicant for VARELISA LA (SS-B) 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 LA (SS-B) ANTIBODIES?
The FDA product code for VARELISA LA (SS-B) 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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