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31 Z3 510(k) Submission The Gluiest Lite/ The Gluiest Lite Professional Blood Glucose Monitoring System 510(k) Summary This summary of 5lO(k)safety and effectiveness information is being submitted
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What is k132966 - accessdata fda?
k132966 - accessdata fda is a unique identifier assigned by the FDA to specific medical devices.
Who is required to file k132966 - accessdata fda?
Manufacturers, distributors, or importers of medical devices are required to file k132966 - accessdata fda.
How to fill out k132966 - accessdata fda?
You can fill out k132966 - accessdata fda online through the FDA's electronic submission system.
What is the purpose of k132966 - accessdata fda?
The purpose of k132966 - accessdata fda is to track and monitor medical devices for safety and effectiveness.
What information must be reported on k132966 - accessdata fda?
Information such as device classification, intended use, and manufacturing details must be reported on k132966 - accessdata fda.
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