K241096
- 510(k) number
- K241096
- Device name
- Venera 608 Deep Vein Thrombosis (DVT) Prevention System
- Applicant
- Suzhou Minhua Medical Apparatus Supplies Co., Ltd. CN
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2025-01-15
- Date received
- 2024-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K241096.pdf
Official FDA record: K241096
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.