meddevicedb.com FDA Device Reference

IGLUCOSE SYSTEM

K111932 Class II Traditional
Decision Date
2011-11-10
Sponsor / Applicant
Positiveid Corporation

Technical Specification

510(k) Submission ID K111932
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2011-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IGLUCOSE SYSTEM received FDA 510(k) clearance under submission number K111932, sponsored by Positiveid Corporation. 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 2011-11-10.

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.