MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST
K-Number: K032235 · 2004-01-28
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST?
MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST is a medical device that received FDA 510(k) clearance on 2004-01-28. The listed applicant is Biosite Incorporated. The 510(k) number is K032235.
When did MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST receive FDA 510(k) clearance?
MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST received FDA 510(k) clearance on 2004-01-28, under 510(k) number K032235.
Who is the listed applicant for MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST?
The FDA 510(k) record lists Biosite Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST?
The FDA product code for MODIFICATION TO TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST 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 Biosite Incorporated 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.
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