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VIDAS CORTISOL (CORT) ASSAY & SERUM FREE DILUTENT

K931031 Class II Traditional
Decision Date
1993-07-27
Sponsor / Applicant
Biomerieux Vitek, Inc.

Technical Specification

510(k) Submission ID K931031
Product Code JFT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1205
Decision Date 1993-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIDAS CORTISOL (CORT) ASSAY & SERUM FREE DILUTENT received FDA 510(k) clearance under submission number K931031, sponsored by Biomerieux Vitek, 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 1993-07-27.

Classification & Regulation

This clearance is catalogued under FDA product code JFT and 21 CFR 862.1205, within the Clinical Chemistry review panel as a Class II device.