meddevicedb.com FDA Device Reference

VENTREZYME T4 IMMUNOASSAY T4

K840473 Class II Traditional
Decision Date
1984-04-04
Sponsor / Applicant
Vxr, Inc.

Technical Specification

510(k) Submission ID K840473
Product Code KLI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1984-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VENTREZYME T4 IMMUNOASSAY T4 received FDA 510(k) clearance under submission number K840473, sponsored by Vxr, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1984-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code KLI and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.