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INDIRECT IMMUNO ENZYME,ANTIGEN,CONTROL

K791749 Class II Traditional
Decision Date
1979-10-17
Sponsor / Applicant
Clinical Sciences, Inc.

Technical Specification

510(k) Submission ID K791749
Product Code DAA
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1979-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INDIRECT IMMUNO ENZYME,ANTIGEN,CONTROL received FDA 510(k) clearance under submission number K791749, sponsored by Clinical Sciences, 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 1979-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code DAA and 21 CFR 866.5510, within the Immunology review panel as a Class II device.