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Omnipod Insulin Management System, Omnipod DASH Insulin Management System

K192659 Class II Traditional
Decision Date
2019-10-21
Sponsor / Applicant
Insulet Corporation

Technical Specification

510(k) Submission ID K192659
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2019-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Omnipod Insulin Management System, Omnipod DASH Insulin Management System received FDA 510(k) clearance under submission number K192659, sponsored by Insulet Corporation. 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 2019-10-21.

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.