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RELISA ENA ANTIBODY SCREENING TEST SYSTEM

K935129 Class II Traditional
Decision Date
1994-01-31
Sponsor / Applicant
Immuno Concepts, Inc.

Technical Specification

510(k) Submission ID K935129
Product Code LLL
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1994-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RELISA ENA ANTIBODY SCREENING TEST SYSTEM received FDA 510(k) clearance under submission number K935129, sponsored by Immuno Concepts, 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 1994-01-31.

Classification & Regulation

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