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ORTHO CLG IMMUNE COMPLEX TEST SYSTEM

K821806 Class II Traditional
Decision Date
1982-06-25
Sponsor / Applicant
Ortho Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K821806
Product Code DAK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5240
Decision Date 1982-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO CLG IMMUNE COMPLEX TEST SYSTEM received FDA 510(k) clearance under submission number K821806, sponsored by Ortho Diagnostic Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1982-06-25.

Classification & Regulation

This clearance is catalogued under FDA product code DAK and 21 CFR 866.5240, within the Immunology review panel as a Class II device.