meddevicedb.com FDA Device Reference

HIGH DENSITY LIPOPROTEIN PRECIPITATIN

K843029 Class I Traditional
Decision Date
1984-08-27
Sponsor / Applicant
Diagnostic Chemicals, Ltd. (Usa)

Technical Specification

510(k) Submission ID K843029
Product Code LBS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1984-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH DENSITY LIPOPROTEIN PRECIPITATIN received FDA 510(k) clearance under submission number K843029, sponsored by Diagnostic Chemicals, Ltd. (Usa). 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 1984-08-27.

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.