TINAQUANT B 2-MICROGLOBULIN ASSAY
K-Number: K980724 · 1998-10-16
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Device Summary
Frequently Asked Questions
What is the TINAQUANT B 2-MICROGLOBULIN ASSAY?
TINAQUANT B 2-MICROGLOBULIN ASSAY is a medical device that received FDA 510(k) clearance on 1998-10-16. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K980724.
When did TINAQUANT B 2-MICROGLOBULIN ASSAY receive FDA 510(k) clearance?
TINAQUANT B 2-MICROGLOBULIN ASSAY received FDA 510(k) clearance on 1998-10-16, under 510(k) number K980724.
Who is the listed applicant for TINAQUANT B 2-MICROGLOBULIN ASSAY?
The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TINAQUANT B 2-MICROGLOBULIN ASSAY?
The FDA product code for TINAQUANT B 2-MICROGLOBULIN ASSAY is JZG.
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 Boehringer Mannheim Corp. 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: JZG)
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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