meddevicedb.com FDA Device Reference

COALIZA PROTEIN S-FREE

K002467 Class II Traditional
Decision Date
2000-10-13
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K002467
Product Code GGP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7290
Decision Date 2000-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COALIZA PROTEIN S-FREE received FDA 510(k) clearance under submission number K002467, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2000-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code GGP and 21 CFR 864.7290, within the Hematology review panel as a Class II device.