ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA
K-Number: K981120 · 1998-08-21
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Device Summary
Frequently Asked Questions
What is the ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA?
ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA is a medical device that received FDA 510(k) clearance on 1998-08-21. The listed applicant is Zeus Scientific, Inc.. The 510(k) number is K981120.
When did ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA receive FDA 510(k) clearance?
ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA received FDA 510(k) clearance on 1998-08-21, under 510(k) number K981120.
Who is the listed applicant for ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA?
The FDA 510(k) record lists Zeus Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA?
The FDA product code for ZEUS SCIENTIFIC INC., ANTI-EBV EA IGG ELISA is LSE.
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 Zeus Scientific, 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: LSE)
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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