Cleared Traditional

K062555 - EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G

K062555 is an FDA 510(k) clearance for EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, manufactured by Visgeneer, Inc.. The device is a Class 2 Chemistry device with product code NBW cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K062555 · Visgeneer, Inc. · Chemistry device
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Dec 2006
Decision
119d
Days
Class 2
Risk

K062555 is an FDA 510(k) clearance for the EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G. Classified as System, Test, Blood Glucose, Over The Counter (product code NBW), Class II - Special Controls.

Submitted by Visgeneer, Inc. (Hsin-Chu City, TW). The FDA issued a Cleared decision on December 27, 2006 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1345 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Visgeneer, Inc. devices

FDA 510(k) Submission Details - K062555

510(k) Number K062555 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 2006
Decision Date December 27, 2006
Days to Decision 119 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d slower than avg
Panel avg: 88d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NBW Device Classification - Class 2, Special Controls

Product Code NBW System, Test, Blood Glucose, Over The Counter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1345
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - NBW System, Test, Blood Glucose, Over The Counter

All 425
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