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FDA 510(k)

Reusable Blood Pressure Cuff

K-Number: K171889 · 2017-12-19

ApplicantSuzhou Minhua Medical Apparatus Supplies Co., Ltd.
Decision Date2017-12-19
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reusable Blood Pressure Cuff is a medical device manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2017-12-19 under approval number K171889. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reusable Blood Pressure Cuff?

Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2017-12-19. It is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K171889.

When was Reusable Blood Pressure Cuff approved by the FDA?

Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2017-12-19, under approval number K171889.

What company makes Reusable Blood Pressure Cuff?

Reusable Blood Pressure Cuff is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd..

What is the FDA product code for Reusable Blood Pressure Cuff?

The FDA product code for Reusable Blood Pressure Cuff is DXQ.

Related Clinical Trials

NCT07260890 Paired Comparison of SVV and PVI Accuracy COMPLETED NCT07613762 High-Flow Nasal Cannula on Exercise Tolerance in Heart Failure Patients Undergoing Cardiac Rehabilitation. NOT_YET_RECRUITING 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 NCT07300878 Effect of Video Laryngoscopy Versus Conventional Laryngoscopy Upon Hemodynamics COMPLETED NCT05707806 Development and Validation of Learning and Decision-Making Tasks 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 Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

K180389Venera 508 Deep Vein Thrombosis (DVT) Prevention System K233276Reusable Blood Pressure Cuff K241096Venera 608 Deep Vein Thrombosis (DVT) Prevention System

Related Devices (Code: DXQ)

K160530Med-link Reusable Blood Pressure Cuff, Med-link Disposable Blood Pressure CuffShenzhen Med-Link Electronics Tech Co., Ltd. K161035Medline Singe Patient Use Blood Pressure CuffMedline Industries, Inc. K152006Cogent Hemodynamic Monitoring SystemIcu Medical, Inc. K153251Tenso TS-101S and TS-101D Disposable Blood Pressure CuffNingbo Free Trade Zone Tenso Medical Instruments Co., Ltd. K173044Reusable Blood Pressure Cuff, Disposable Blood Pressure CuffNingbo Albert Novosino Co., Ltd. K182433Reusable Blood Pressure Cuff, Disposable Blood Pressure CuffShenzhen Caremed Medical Technology 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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