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Insulia Diabetes Management Companion

K170669 Class II Traditional
Decision Date
2017-06-19
Sponsor / Applicant
Voluntis Sa.

Technical Specification

510(k) Submission ID K170669
Product Code NDC
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1890
Decision Date 2017-06-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Insulia Diabetes Management Companion received FDA 510(k) clearance under submission number K170669, sponsored by Voluntis Sa.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2017-06-19.

Classification & Regulation

This clearance is catalogued under FDA product code NDC and 21 CFR 868.1890, within the Anesthesiology review panel as a Class II device.