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ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL

K051733 Class II Traditional
Decision Date
2005-12-07
Sponsor / Applicant
Drg Intl., Inc.

Technical Specification

510(k) Submission ID K051733
Product Code NHG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1205
Decision Date 2005-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL received FDA 510(k) clearance under submission number K051733, sponsored by Drg Intl., 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 2005-12-07.

Classification & Regulation

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