meddevicedb.com FDA Device Reference

LIPOPRINT SYSTEM, LDL SUBFRACTIONS

K010337 Class I Traditional
Decision Date
2001-07-25
Sponsor / Applicant
Quantimetrix Corp.

Technical Specification

510(k) Submission ID K010337
Product Code JHO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 2001-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPOPRINT SYSTEM, LDL SUBFRACTIONS received FDA 510(k) clearance under submission number K010337, sponsored by Quantimetrix 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 2001-07-25.

Classification & Regulation

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