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FDA 510(k)

Blood Pressure Monitor

K-Number: K233130 · 2023-12-20

ApplicantGuangdong Transtek Medical Electronics Co., Ltd.
Decision Date2023-12-20
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Blood Pressure Monitor is a medical device manufactured by Guangdong Transtek Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2023-12-20 under approval number K233130. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Blood Pressure Monitor?

Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2023-12-20. It is manufactured by Guangdong Transtek Medical Electronics Co., Ltd.. The 510(k) number is K233130.

When was Blood Pressure Monitor approved by the FDA?

Blood Pressure Monitor received FDA 510(k) clearance on 2023-12-20, under approval number K233130.

What company makes Blood Pressure Monitor?

Blood Pressure Monitor is manufactured by Guangdong Transtek Medical Electronics Co., Ltd..

What is the FDA product code for Blood Pressure Monitor?

The FDA product code for Blood Pressure Monitor is DXN.

Related Clinical Trials

NCT07260890 Paired Comparison of SVV and PVI Accuracy COMPLETED NCT07614139 Continuous Glucose Monitoring Alerts, Accuracy, and Patient Outcomes in Adults With Inherited Metabolic Disorders COMPLETED NCT07613762 High-Flow Nasal Cannula on Exercise Tolerance in Heart Failure Patients Undergoing Cardiac Rehabilitation. NOT_YET_RECRUITING NCT06940752 VINTAGE (Ventricular Intramyocardial Navigation for Tachycardia Ablation Guided by Electrograms) Using Commercial Off-The-Shelf (COTS) Catheters ENROLLING_BY_INVITATION NCT07499128 Continuous Temperature Monitoring (CTM) for Cytokine Release Syndrome (CRS), an Immune-Related Adverse Event ENROLLING_BY_INVITATION NCT07099092 Causal Mechanisms of Odor-Guided Behavior in Humans NOT_YET_RECRUITING

Related PubMed Literature

PMID: 41836285 A Case Study of AI-Enabled Software as a Medical Device Cleared by the FDA for Assessing Hemorrhage Risk Index (APPRAISE-HRI) after Trauma. NEJM AI (2025) PMID: 41623865 Case Report: Hypertensive encephalopathy presents with complex types of sleep breathing events. Frontiers in cardiovascular medicine (2025)

Other Devices by Guangdong Transtek Medical Electronics Co., Ltd.

K161886Transtek Blood Pressure Monitor, Welch Allyn Remote Monitoring Blood Pressure Device, Welch Allyn Home Blood Pressure Device K181832Transtek Blood Pressure Monitor; Welch Allyn 901123 Digital Blood Pressure Device K202599Transtek Wrist Blood Pressure Monitor K202891Blood Pressure Monitor K220676Blood Pressure Monitor K232713Blood Pressure Monitor

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Related Devices (Code: DXN)

K162092Evolv Model BP7000 Upper Arm Blood Pressure MonitorOmron Healthcare, Inc. K161708Arm automatic blood pressure monitorShenzhen Pump Medical System Co., Ltd. K162230Fully Automatic Electronic Blood Pressure MonitorAdon Health Co., Ltd. K160349Electronic SphygmomanometerGuangdong Biolight Meditech Co., Ltd. K161846Automatic Arm Bluetooth Blood Pressure MonitorTruly Instrument Limited K161886Transtek Blood Pressure Monitor, Welch Allyn Remote Monitoring Blood Pressure Device, Welch Allyn Home Blood Pressure DeviceGuangdong Transtek Medical Electronics 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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