Cleared Abbreviated

K091296 - POLYTEL GMA, MODELS PWR-08-67, PWR-08-07, PWR-08-09

K091296 is an FDA 510(k) clearance for POLYTEL GMA, manufactured by Polymap Wireless. The device is a Class 2 Chemistry device with product code NBW cleared through the Abbreviated 510(k) pathway after a 74-day FDA review.

K091296 · Polymap Wireless · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2009
Decision
74d
Days
Class 2
Risk

K091296 is an FDA 510(k) clearance for the POLYTEL GMA, MODELS PWR-08-67, PWR-08-07, PWR-08-09. Classified as System, Test, Blood Glucose, Over The Counter (product code NBW), Class II - Special Controls.

Submitted by Polymap Wireless (Tucson, US). The FDA issued a Cleared decision on July 17, 2009 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1345 - the FDA in vitro diagnostics and chemistry framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Polymap Wireless devices

FDA 510(k) Submission Details - K091296

510(k) Number K091296 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 04, 2009
Decision Date July 17, 2009
Days to Decision 74 days
Submission Type Abbreviated
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d faster than avg
Panel avg: 88d · This submission: 74d
Pathway characteristics
Standards-based clearance path.

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 310
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