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FDA 510(k)

Smart Dongle Blood Glucose Monitoring System

K-Number: K162382 · 2017-04-14

ApplicantTaidoc Technology Corporation
Decision Date2017-04-14
Product CodeNBW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Smart Dongle Blood Glucose Monitoring System is a medical device manufactured by Taidoc Technology Corporation. It received FDA 510(k) clearance on 2017-04-14 under approval number K162382. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Smart Dongle Blood Glucose Monitoring System?

Smart Dongle Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-04-14. It is manufactured by Taidoc Technology Corporation. The 510(k) number is K162382.

When was Smart Dongle Blood Glucose Monitoring System approved by the FDA?

Smart Dongle Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-04-14, under approval number K162382.

What company makes Smart Dongle Blood Glucose Monitoring System?

Smart Dongle Blood Glucose Monitoring System is manufactured by Taidoc Technology Corporation.

What is the FDA product code for Smart Dongle Blood Glucose Monitoring System?

The FDA product code for Smart Dongle Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.

Related Clinical Trials

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Related PubMed Literature

PMID: 42174947 Aligning AI-Native 6G Healthcare Systems with EU Ethical and Legal Frameworks. Studies in health technology and informatics (2026) PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026) PMID: 41964171 Journal of diabetes science and technology (2026) PMID: 41760572 Trends in use of continuous glucose monitors among individuals with type 2 diabetes enrolled in Medicare Advantage (2021-2023). Journal of managed care & specialty pharmacy (2026)

Other Devices by Taidoc Technology Corporation

K161738FORA ADVANCED GD40 and FORA ADVANCED GD40 pro Blood Glucose and ß-Ketone Monitoring Systems K152680TD-1035 Thermometer K151024Finger Type Pulse Oximeter K142664URight Hemoglobin A1c system, FORA A1c System K180863FORA NAS100 Electronic Nasal Aspirator, Electronic Nasal Aspirator K181675FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System

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Related Devices (Code: NBW)

K161299BGM014 Blood Glucose Monitoring System, BGM014 Pro Blood Glucose Monitoring SystemApex BioTechnology Corp. K160742NoCoding1 Plus Blood Glucose Monitoring SystemI-Sens, Inc. K161834One Drop Blood Glucose Monitoring SystemAgamatrix, Inc. K160682CONTOUR NEXT ONE Blood Glucose Monitoring SystemAscensia Diabetes Care K161738FORA ADVANCED GD40 and FORA ADVANCED GD40 pro Blood Glucose and ß-Ketone Monitoring SystemsTaidoc Technology Corporation K160365BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring SystemInfopia Co, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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