meddevicedb.com FDA Device Reference

STRATUS(R) THYROID UPTAKE FLUOR ENZYME IMMUNOASSAY

K933414 Class II Traditional
Decision Date
1994-11-22
Sponsor / Applicant
Baxter Diagnostics, Inc.

Technical Specification

510(k) Submission ID K933414
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1994-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRATUS(R) THYROID UPTAKE FLUOR ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K933414, sponsored by Baxter Diagnostics, 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 1994-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.