AXSYM RUBELLA IGG ANTIBODY ASSAY
K-Number: K954045 · 1996-09-24
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Device Summary
Frequently Asked Questions
What is the AXSYM RUBELLA IGG ANTIBODY ASSAY?
AXSYM RUBELLA IGG ANTIBODY ASSAY is a medical device that received FDA 510(k) clearance on 1996-09-24. The listed applicant is Abbott Laboratories. The 510(k) number is K954045.
When did AXSYM RUBELLA IGG ANTIBODY ASSAY receive FDA 510(k) clearance?
AXSYM RUBELLA IGG ANTIBODY ASSAY received FDA 510(k) clearance on 1996-09-24, under 510(k) number K954045.
Who is the listed applicant for AXSYM RUBELLA IGG ANTIBODY ASSAY?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXSYM RUBELLA IGG ANTIBODY ASSAY?
The FDA product code for AXSYM RUBELLA IGG ANTIBODY ASSAY is LFX.
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 Abbott Laboratories 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: LFX)
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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