VITEK 2 AST-ST TIGECYCLINE
K-Number: K131779 · 2013-10-10
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Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-ST TIGECYCLINE?
VITEK 2 AST-ST TIGECYCLINE is a medical device that received FDA 510(k) clearance on 2013-10-10. The listed applicant is bioMerieux, Inc.. The 510(k) number is K131779.
When did VITEK 2 AST-ST TIGECYCLINE receive FDA 510(k) clearance?
VITEK 2 AST-ST TIGECYCLINE received FDA 510(k) clearance on 2013-10-10, under 510(k) number K131779.
Who is the listed applicant for VITEK 2 AST-ST TIGECYCLINE?
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 AST-ST TIGECYCLINE?
The FDA product code for VITEK 2 AST-ST TIGECYCLINE 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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