meddevicedb.com FDA Device Reference

TOTAL CHOLESTEROL AND HDL CHOLESTEROL PANEL

K946063 Class I Traditional
Decision Date
1995-02-22
Sponsor / Applicant
Cholestech Corp.

Technical Specification

510(k) Submission ID K946063
Product Code CHH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1175
Decision Date 1995-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL CHOLESTEROL AND HDL CHOLESTEROL PANEL received FDA 510(k) clearance under submission number K946063, sponsored by Cholestech 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 1995-02-22.

Classification & Regulation

This clearance is catalogued under FDA product code CHH and 21 CFR 862.1175, within the Clinical Chemistry review panel as a Class I device.