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FDA 510(k)

TINAQUANT B 2-MICROGLOBULIN ASSAY

K-Number: K980724 · 1998-10-16

Decision Date1998-10-16
Product CodeJZG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TINAQUANT B 2-MICROGLOBULIN ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1998-10-16 under 510(k) number K980724. The device is classified under product code JZG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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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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