K232640
- 510(k) number
- K232640
- Device name
- Venowave VW5
- Applicant
- Thermabright OH · US
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2024-06-25
- Date received
- 2023-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K232640.pdf
Official FDA record: K232640
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.