510(k) K243060

Device
TeleRPM Gen2 Blood Glucose Monitoring System
Applicant
Guangdong Transtek Medical Electronics Co., Ltd.
510(k) number
K243060
Product code
NBW
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-30
Date received
2024-09-27
Regulation
862.1345
Classification name
System, Test, Blood Glucose, Over The Counter
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Qian Mark
Address
Zone A, # 105, Dongli Rd., Torch Development District Zhongshan CN 528437 528437

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K233058VivaChek Link Plus Blood Glucose Monitoring SystemVivachek Biotech (Hangzhou) Co., Ltd.2023-12-22
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K213131Accu-Chek Guide Solo diabetes manager blood glucose monitoring systemRoche Diabetes Care GmbH2023-08-10
K223722MIO Blood Glucose Monitoring SystemMio Labs, Inc.2023-06-28
K222234GlucoSure ADVANCE Link Blood Glucose Monitoring SystemApex BioTechnology Corp.2022-12-21
K223293CONTOUR® NEXT GEN Blood Glucose Monitoring SystemAscensia Diabetes Care U.S., Inc.2022-11-18