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e-CFR data is current as of November 20, 2020

Title 21Chapter ISubchapter HPart 866Subpart G → §866.6030

Title 21: Food and Drugs
Subpart G—Tumor Associated Antigen immunological Test Systems

§866.6030   AFP-L3% immunological test system.

(a) Identification. An AFP-L3% immunological test system is an in vitro device that consists of reagents and an automated instrument used to quantitatively measure, by immunochemical techniques, AFP and AFP-L3 subfraction in human serum. The device is intended for in vitro diagnostic use as an aid in the risk assessment of patients with chronic liver disease for development of hepatocellular carcinoma, in conjunction with other laboratory findings, imaging studies, and clinical assessment.

(b) Classification. Class II (special controls). The special control is FDA's guidance document entitled “Class II Special Controls Guidance Document: AFP-L3% Immunological Test Systems.” See §866.1(e) for the availability of this guidance document.

[70 FR 57749, Oct. 4, 2005]

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