Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2025-01-15 under 510(k) 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. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K241096.

When did Venera 608 Deep Vein Thrombosis (DVT) Prevention System receive FDA 510(k) clearance?

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

Who is the listed applicant for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA 510(k) record lists Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.