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ACCU-CHEK CONNECT DIABETES MANAGEMENT APP

K141929 Class II Traditional
Decision Date
2015-03-16
Sponsor / Applicant
Roche Diagnostics Corporation

Technical Specification

510(k) Submission ID K141929
Product Code NDC
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1890
Decision Date 2015-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCU-CHEK CONNECT DIABETES MANAGEMENT APP received FDA 510(k) clearance under submission number K141929, sponsored by Roche Diagnostics Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2015-03-16.

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.