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LIPIDIRECT LOW DENSITY LIPOPROTEIN CHOLESTEROL TES

K893740 Class I Traditional
Decision Date
1990-03-19
Sponsor / Applicant
Reference Diagnostics, Inc.

Technical Specification

510(k) Submission ID K893740
Product Code MRR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1990-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPIDIRECT LOW DENSITY LIPOPROTEIN CHOLESTEROL TES received FDA 510(k) clearance under submission number K893740, sponsored by Reference 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 1990-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code MRR and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.