Venera 608 Deep Vein Thrombosis (DVT) Prevention System— 510(k) K241096

Name: FDA 510(k) clearance K241096
Creator: U.S. Food and Drug Administration
Published: 2025-01-15

Substantially Equivalent

Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

FDA 510(k) clearance K241096 for Venera 608 Deep Vein Thrombosis (DVT) Prevention System, Substantially Equivalent on 2025-01-15. Applicant: Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. Device class: 2.

Clearance details

Applicant: Suzhou Minhua Medical Apparatus Supplies Co., Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2024-04-22
Decision date: 2025-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suzhou, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.