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BOEHRINGER MANNHEIM DIRECT HDL-CHOLESTEROL

K970735 Class I Traditional
Decision Date
1997-06-06
Sponsor / Applicant
Randox Laboratories, Ltd.

Technical Specification

510(k) Submission ID K970735
Product Code LBS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1997-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOEHRINGER MANNHEIM DIRECT HDL-CHOLESTEROL received FDA 510(k) clearance under submission number K970735, sponsored by Randox Laboratories, Ltd.. 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 1997-06-06.

Classification & Regulation

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