DAKO ITA, IMMUNOGLOBULIN A (IGA)
K-Number: K862183 · 1986-08-19
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Device Summary
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.
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
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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