IGA IMMUNOTURBIDIMETRIC & CALIBRATOR
K-Number: K955794 · 1996-04-05
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Device Summary
Frequently Asked Questions
What is the IGA IMMUNOTURBIDIMETRIC & CALIBRATOR?
IGA IMMUNOTURBIDIMETRIC & CALIBRATOR is a medical device that received FDA 510(k) clearance on 1996-04-05. The listed applicant is Randox Laboratories, Ltd.. The 510(k) number is K955794.
When did IGA IMMUNOTURBIDIMETRIC & CALIBRATOR receive FDA 510(k) clearance?
IGA IMMUNOTURBIDIMETRIC & CALIBRATOR received FDA 510(k) clearance on 1996-04-05, under 510(k) number K955794.
Who is the listed applicant for IGA IMMUNOTURBIDIMETRIC & CALIBRATOR?
The FDA 510(k) record lists Randox Laboratories, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IGA IMMUNOTURBIDIMETRIC & CALIBRATOR?
The FDA product code for IGA IMMUNOTURBIDIMETRIC & CALIBRATOR 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 Randox Laboratories, Ltd. 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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