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FDA 510(k)

DAKO ITA, IMMUNOGLOBULIN A (IGA)

K-Number: K862183 · 1986-08-19

ApplicantDako Corp.
Decision Date1986-08-19
Product CodeCZP
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DAKO ITA, IMMUNOGLOBULIN A (IGA) is the device name listed in this FDA 510(k) record. The listed applicant is Dako Corp.. It received FDA 510(k) clearance on 1986-08-19 under 510(k) number K862183. The device is classified under product code CZP. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAKO ITA, IMMUNOGLOBULIN A (IGA)?

DAKO ITA, IMMUNOGLOBULIN A (IGA) is a medical device that received FDA 510(k) clearance on 1986-08-19. The listed applicant is Dako Corp.. The 510(k) number is K862183.

When did DAKO ITA, IMMUNOGLOBULIN A (IGA) receive FDA 510(k) clearance?

DAKO ITA, IMMUNOGLOBULIN A (IGA) received FDA 510(k) clearance on 1986-08-19, under 510(k) number K862183.

Who is the listed applicant for DAKO ITA, IMMUNOGLOBULIN A (IGA)?

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

What is the FDA product code for DAKO ITA, IMMUNOGLOBULIN A (IGA)?

The FDA product code for DAKO ITA, IMMUNOGLOBULIN A (IGA) is CZP.

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 Dako 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.

View all 54 devices →

Related Devices (Code: CZP)

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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