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FreeStyle Precision Neo H Blood Glucose Monitoring System

K153330 Class II Traditional
Decision Date
2016-02-19
Sponsor / Applicant
Abbott Diabetes Care, Inc.

Technical Specification

510(k) Submission ID K153330
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2016-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FreeStyle Precision Neo H Blood Glucose Monitoring System received FDA 510(k) clearance under submission number K153330, sponsored by Abbott Diabetes Care, 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 2016-02-19.

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.