meddevicedb.com FDA Device Reference

EASYRA CLINICAL CHEMISTRY ANALYZER

K070057 Class II Traditional
Decision Date
2007-08-30
Sponsor / Applicant
Medica Corp.

Technical Specification

510(k) Submission ID K070057
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2007-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYRA CLINICAL CHEMISTRY ANALYZER received FDA 510(k) clearance under submission number K070057, sponsored by Medica 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 2007-08-30.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.