meddevicedb.com FDA Device Reference

GlucoSure ADVANCE Link Blood Glucose Monitoring System

K222234 Class II Special
Decision Date
2022-12-21
Sponsor / Applicant
Apex BioTechnology Corp.

Technical Specification

510(k) Submission ID K222234
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2022-12-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GlucoSure ADVANCE Link Blood Glucose Monitoring System received FDA 510(k) clearance under submission number K222234, sponsored by Apex BioTechnology Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2022-12-21.

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.