Cleared Traditional

K160156 - StatStrip Xpress Blood Glucose Monitoring System (FDA 510(k) Clearance)

Jun 2016
Decision
153d
Days
Class 2
Risk

K160156 is an FDA 510(k) clearance for the StatStrip Xpress Blood Glucose Monitoring System. This device is classified as a System, Test, Blood Glucose, Over The Counter (Class II - Special Controls, product code NBW).

Submitted by Nova Biomedical Corporation (Walham, US). The FDA issued a Cleared decision on June 23, 2016, 153 days after receiving the submission on January 22, 2016.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1345.

Submission Details

510(k) Number K160156 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 2016
Decision Date June 23, 2016
Days to Decision 153 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code NBW — System, Test, Blood Glucose, Over The Counter
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1345

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