VITEK 2 ESBL TEST
K-Number: K040845 · 2004-06-08
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Device Summary
Frequently Asked Questions
What is the VITEK 2 ESBL TEST?
VITEK 2 ESBL TEST is a medical device that received FDA 510(k) clearance on 2004-06-08. The listed applicant is bioMerieux, Inc.. The 510(k) number is K040845.
When did VITEK 2 ESBL TEST receive FDA 510(k) clearance?
VITEK 2 ESBL TEST received FDA 510(k) clearance on 2004-06-08, under 510(k) number K040845.
Who is the listed applicant for VITEK 2 ESBL TEST?
The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITEK 2 ESBL TEST?
The FDA product code for VITEK 2 ESBL TEST is LON.
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 bioMerieux, 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: LON)
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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