meddevicedb.com FDA Device Reference

EASYGLUCO, MODEL IGM0002

K031501 Class II Traditional
Decision Date
2003-10-16
Sponsor / Applicant
American Healthcare, Inc.

Technical Specification

510(k) Submission ID K031501
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2003-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYGLUCO, MODEL IGM0002 received FDA 510(k) clearance under submission number K031501, sponsored by American Healthcare, Inc.. 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 2003-10-16.

Classification & Regulation

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