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NML CORTISOL RIA

K840466 Class II Traditional
Decision Date
1984-03-30
Sponsor / Applicant
Nuclear Medical Laboratories, Inc.

Technical Specification

510(k) Submission ID K840466
Product Code CGR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1205
Decision Date 1984-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NML CORTISOL RIA received FDA 510(k) clearance under submission number K840466, sponsored by Nuclear Medical Laboratories, 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 1984-03-30.

Classification & Regulation

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