meddevicedb.com FDA Device Reference

CARESENS N VOICE BLOOD GLUCOSE MONITORING SYSTEM

K121133 Class II Special
Decision Date
2012-07-10
Sponsor / Applicant
I-Sens, Inc.

Technical Specification

510(k) Submission ID K121133
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2012-07-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARESENS N VOICE BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance under submission number K121133, sponsored by I-Sens, Inc.. 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 2012-07-10.

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.