BETA-2 MICROGLOBULIN EIA
K-Number: K901333 · 1990-04-02
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Device Summary
Frequently Asked Questions
What is the BETA-2 MICROGLOBULIN EIA?
BETA-2 MICROGLOBULIN EIA is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is Serex, Inc.. The 510(k) number is K901333.
When did BETA-2 MICROGLOBULIN EIA receive FDA 510(k) clearance?
BETA-2 MICROGLOBULIN EIA received FDA 510(k) clearance on 1990-04-02, under 510(k) number K901333.
Who is the listed applicant for BETA-2 MICROGLOBULIN EIA?
The FDA 510(k) record lists Serex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BETA-2 MICROGLOBULIN EIA?
The FDA product code for BETA-2 MICROGLOBULIN EIA is JZG.
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 Serex, 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: JZG)
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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