N LATEX B2-MICROGLOBULIN
K-Number: K002731 · 2000-11-20
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Device Summary
Frequently Asked Questions
What is the N LATEX B2-MICROGLOBULIN?
N LATEX B2-MICROGLOBULIN is a medical device that received FDA 510(k) clearance on 2000-11-20. The listed applicant is Dade Behring, Inc.. The 510(k) number is K002731.
When did N LATEX B2-MICROGLOBULIN receive FDA 510(k) clearance?
N LATEX B2-MICROGLOBULIN received FDA 510(k) clearance on 2000-11-20, under 510(k) number K002731.
Who is the listed applicant for N LATEX B2-MICROGLOBULIN?
The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for N LATEX B2-MICROGLOBULIN?
The FDA product code for N LATEX B2-MICROGLOBULIN 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 Dade Behring, 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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