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ST AIA-PACK AFP ENZYME IMMUNOASSAY

K023894 Class II Special
Decision Date
2002-12-17
Sponsor / Applicant
Tosoh Medics, Inc.

Technical Specification

510(k) Submission ID K023894
Product Code LOJ
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6010
Decision Date 2002-12-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ST AIA-PACK AFP ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K023894, sponsored by Tosoh Medics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2002-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code LOJ and 21 CFR 866.6010, within the Immunology review panel as a Class II device.