EBNA ACIF ASSAY KIT
K-Number: K871298 · 1987-06-25
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Device Summary
Frequently Asked Questions
What is the EBNA ACIF ASSAY KIT?
EBNA ACIF ASSAY KIT is a medical device that received FDA 510(k) clearance on 1987-06-25. The listed applicant is Granbio, Inc.. The 510(k) number is K871298.
When did EBNA ACIF ASSAY KIT receive FDA 510(k) clearance?
EBNA ACIF ASSAY KIT received FDA 510(k) clearance on 1987-06-25, under 510(k) number K871298.
Who is the listed applicant for EBNA ACIF ASSAY KIT?
The FDA 510(k) record lists Granbio, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EBNA ACIF ASSAY KIT?
The FDA product code for EBNA ACIF ASSAY KIT is LLM.
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 Granbio, 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: LLM)
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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