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StatStrip Xpress Glucose Hospital Meter System

K161856 Class II Special
Decision Date
2016-11-15
Sponsor / Applicant
Nova Biomedical Corporation

Technical Specification

510(k) Submission ID K161856
Product Code PZI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2016-11-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

StatStrip Xpress Glucose Hospital Meter System received FDA 510(k) clearance under submission number K161856, sponsored by Nova Biomedical Corporation. 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 2016-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code PZI and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.