meddevicedb.com FDA Device Reference

LIGAND PLUS CONTROL LEVEL 1-3

K033344 Class I Traditional
Decision Date
2004-01-16
Sponsor / Applicant
Consolidated Technology

Technical Specification

510(k) Submission ID K033344
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2004-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIGAND PLUS CONTROL LEVEL 1-3 received FDA 510(k) clearance under submission number K033344, sponsored by Consolidated Technology. 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 2004-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.