VIDAS NT-PROBNP ASSAY, MODEL: 30 449
K-Number: K073091 · 2008-02-29
Advertisement
Device Summary
Frequently Asked Questions
What is the VIDAS NT-PROBNP ASSAY, MODEL: 30 449?
VIDAS NT-PROBNP ASSAY, MODEL: 30 449 is a medical device that received FDA 510(k) clearance on 2008-02-29. The listed applicant is bioMerieux, Inc.. The 510(k) number is K073091.
When did VIDAS NT-PROBNP ASSAY, MODEL: 30 449 receive FDA 510(k) clearance?
VIDAS NT-PROBNP ASSAY, MODEL: 30 449 received FDA 510(k) clearance on 2008-02-29, under 510(k) number K073091.
Who is the listed applicant for VIDAS NT-PROBNP ASSAY, MODEL: 30 449?
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 VIDAS NT-PROBNP ASSAY, MODEL: 30 449?
The FDA product code for VIDAS NT-PROBNP ASSAY, MODEL: 30 449 is NBC.
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: NBC)
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.
Advertisement