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V-TREND TARGET CRP TEST

K890423 Class II Traditional
Decision Date
1989-02-17
Sponsor / Applicant
Texas Immunology, Inc.

Technical Specification

510(k) Submission ID K890423
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 1989-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V-TREND TARGET CRP TEST received FDA 510(k) clearance under submission number K890423, sponsored by Texas Immunology, 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 1989-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code DCK and 21 CFR 866.5270, within the Immunology review panel as a Class II device.