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FDA 510(k)

IMX CMV IGM ANTIBODY ASSAY

K-Number: K900473 · 1990-07-27

Decision Date1990-07-27
Product CodeLFZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IMX CMV IGM ANTIBODY ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K900473. The device is classified under product code LFZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMX CMV IGM ANTIBODY ASSAY?

IMX CMV IGM ANTIBODY ASSAY is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Abbott Laboratories. The 510(k) number is K900473.

When did IMX CMV IGM ANTIBODY ASSAY receive FDA 510(k) clearance?

IMX CMV IGM ANTIBODY ASSAY received FDA 510(k) clearance on 1990-07-27, under 510(k) number K900473.

Who is the listed applicant for IMX CMV IGM ANTIBODY ASSAY?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMX CMV IGM ANTIBODY ASSAY?

The FDA product code for IMX CMV IGM ANTIBODY ASSAY is LFZ.

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 Abbott Laboratories 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: LFZ)

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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