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FDA 510(k)

VITEK 2 ESBL TEST

K-Number: K040845 · 2004-06-08

Decision Date2004-06-08
Product CodeLON
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK 2 ESBL TEST is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 2004-06-08 under 510(k) number K040845. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 248 devices →

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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