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ORGENTEC ANTI-SCL 70 ELISA

K962055 Class II Traditional
Decision Date
1996-11-15
Sponsor / Applicant
American Laboratory Products Co., Ltd.

Technical Specification

510(k) Submission ID K962055
Product Code LJM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1996-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORGENTEC ANTI-SCL 70 ELISA received FDA 510(k) clearance under submission number K962055, sponsored by American Laboratory Products Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1996-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code LJM and 21 CFR 866.5100, within the Immunology review panel as a Class II device.