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ORGEN TEC ANTI-DSDNA PIN IMMUNO ASSAY

K952055 Class II Traditional
Decision Date
1995-07-18
Sponsor / Applicant
American Laboratory Products Co., Ltd.

Technical Specification

510(k) Submission ID K952055
Product Code LRM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1995-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORGEN TEC ANTI-DSDNA PIN IMMUNO ASSAY received FDA 510(k) clearance under submission number K952055, 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 1995-07-18.

Classification & Regulation

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