meddevicedb.com FDA Device Reference

ARK CARE DIABETES MANAGMENT SYSTEM

K110709 Class II Traditional
Decision Date
2011-05-19
Sponsor / Applicant
Arkray Factory USA, Inc.

Technical Specification

510(k) Submission ID K110709
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2011-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARK CARE DIABETES MANAGMENT SYSTEM received FDA 510(k) clearance under submission number K110709, sponsored by Arkray Factory USA, Inc.. 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 2011-05-19.

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.