K241096 is an FDA 510(k) clearance for the Venera 608 Deep Vein Thrombosis (DVT) Prevention System. This device is classified as a Sleeve, Limb, Compressible (Class II - Special Controls, product code JOW).
Submitted by Suzhou Minhua Medical Apparatus Supplies Co., Ltd. (Suzhou, CN). The FDA issued a Cleared decision on January 15, 2025, 268 days after receiving the submission on April 22, 2024.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.5800.
| 510(k) Number | K241096 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 22, 2024 |
| Decision Date | January 15, 2025 |
| Days to Decision | 268 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | JOW - Sleeve, Limb, Compressible |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.5800 |