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FDA 510(k)

Venera 608 Deep Vein Thrombosis (DVT) Prevention System

K-Number: K241096 · 2025-01-15

Decision Date2025-01-15
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is a medical device manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2025-01-15 under approval number K241096. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is a medical device that received FDA 510(k) clearance on 2025-01-15. It is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K241096.

When was Venera 608 Deep Vein Thrombosis (DVT) Prevention System approved by the FDA?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System received FDA 510(k) clearance on 2025-01-15, under approval number K241096.

What company makes Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd..

What is the FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System is JOW.

Related Clinical Trials

Other Devices by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

Related Devices (Code: JOW)

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.