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FDA 510(k)

VITEK 2 STRPTOCOCCUS AMPICILLIN

K-Number: K112075 · 2011-09-15

Decision Date2011-09-15
Product CodeLON
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK 2 STRPTOCOCCUS AMPICILLIN is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 2011-09-15 under 510(k) number K112075. 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 STRPTOCOCCUS AMPICILLIN?

VITEK 2 STRPTOCOCCUS AMPICILLIN is a medical device that received FDA 510(k) clearance on 2011-09-15. The listed applicant is bioMerieux, Inc.. The 510(k) number is K112075.

When did VITEK 2 STRPTOCOCCUS AMPICILLIN receive FDA 510(k) clearance?

VITEK 2 STRPTOCOCCUS AMPICILLIN received FDA 510(k) clearance on 2011-09-15, under 510(k) number K112075.

Who is the listed applicant for VITEK 2 STRPTOCOCCUS AMPICILLIN?

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 STRPTOCOCCUS AMPICILLIN?

The FDA product code for VITEK 2 STRPTOCOCCUS AMPICILLIN 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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