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PDC HDL EZ-SEP CHOLESTEROL REAGENT

K840676 Class I Traditional
Decision Date
1984-04-04
Sponsor / Applicant
Preventive Diagnostics Corp.

Technical Specification

510(k) Submission ID K840676
Product Code LBS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1984-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PDC HDL EZ-SEP CHOLESTEROL REAGENT received FDA 510(k) clearance under submission number K840676, sponsored by Preventive Diagnostics Corp.. 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 1984-04-04.

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.