FDA 510(k)

WowGoHealth Blood Glucose Monitoring System

K-Number: K171785 · 2017-09-15

Decision Date2017-09-15

Product CodeNBW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

WowGoHealth Blood Glucose Monitoring System is a medical device manufactured by Biotest Medical Corporation. It received FDA 510(k) clearance on 2017-09-15 under approval number K171785. 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 WowGoHealth Blood Glucose Monitoring System?

WowGoHealth Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-09-15. It is manufactured by Biotest Medical Corporation. The 510(k) number is K171785.

When was WowGoHealth Blood Glucose Monitoring System approved by the FDA?

WowGoHealth Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-09-15, under approval number K171785.

What company makes WowGoHealth Blood Glucose Monitoring System?

WowGoHealth Blood Glucose Monitoring System is manufactured by Biotest Medical Corporation.

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

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

Related Clinical Trials

NCT01143558 Searching for Persistence of Infection in Lyme Disease COMPLETED NCT07614139 Continuous Glucose Monitoring Alerts, Accuracy, and Patient Outcomes in Adults With Inherited Metabolic Disorders COMPLETED NCT06727942 Virtual Reality-Infused Treadmill Training on Aging-Related Outcomes RECRUITING NCT01143454 Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System RECRUITING NCT01174108 Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells RECRUITING NCT07614100 Cerebral Microembolization During Transcatheter Aortic Valve Implantation: Comparing Balloon-expandable and Self-expanding Valves NOT_YET_RECRUITING

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 Biotest Medical Corporation

K171822NuvoMed Wireless Blood Glucose Monitoring System (Model BGM-6/0352)

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.