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IXL DIABETES MANAGEMENT SYSTEM

K031373 Class II Traditional
Decision Date
2003-12-19
Sponsor / Applicant
Insulet Corp.

Technical Specification

510(k) Submission ID K031373
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2003-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IXL DIABETES MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K031373, sponsored by Insulet Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2003-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code LZG and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.