Cleared Traditional

TeleRPM Gen2 Blood Glucose Monitoring System

Jan 2025
Decision
125d
Days
Class 2
Risk

About This 510(k) Submission

K243060 is an FDA 510(k) clearance for the TeleRPM Gen2 Blood Glucose Monitoring System, a System, Test, Blood Glucose, Over The Counter (Class II — Special Controls, product code NBW), submitted by Guangdong Transtek Medical Electronics Co., Ltd. (Zhongshan, CN). The FDA issued a Cleared decision on January 30, 2025, 125 days after receiving the submission on September 27, 2024. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1345.

Submission Details

510(k) Number K243060 FDA.gov
FDA Decision Cleared SESE
Date Received September 27, 2024
Decision Date January 30, 2025
Days to Decision 125 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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