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FDA 510(k)

QUANTA LITE B2 GPI IGA

K-Number: K973006 · 1997-10-20

Decision Date1997-10-20
Product CodeMSV
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE B2 GPI IGA is the device name listed in this FDA 510(k) record. The listed applicant is Inova Diagnostics, Inc.. It received FDA 510(k) clearance on 1997-10-20 under 510(k) number K973006. The device is classified under product code MSV. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTA LITE B2 GPI IGA?

QUANTA LITE B2 GPI IGA is a medical device that received FDA 510(k) clearance on 1997-10-20. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K973006.

When did QUANTA LITE B2 GPI IGA receive FDA 510(k) clearance?

QUANTA LITE B2 GPI IGA received FDA 510(k) clearance on 1997-10-20, under 510(k) number K973006.

Who is the listed applicant for QUANTA LITE B2 GPI IGA?

The FDA 510(k) record lists Inova Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTA LITE B2 GPI IGA?

The FDA product code for QUANTA LITE B2 GPI IGA is MSV.

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 Inova Diagnostics, 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.

View all 127 devices →

Related Devices (Code: MSV)

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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