Venera 608 Deep Vein Thrombosis (DVT) Prevention System (K241096)
Description
Venera 608 Deep Vein Thrombosis (DVT) Prevention System by Suzhou Minhua Medical Apparatus Supplies Co., Ltd., an FDA 510(k) cleared cardiovascular device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241096
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Venera 608 Deep Vein Thrombosis (DVT) Prevention System (K241096) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K141578 | DEVON CIRONA 6200 DVT | Devon Medical | 2014 |
Trace the full predicate network for K241096
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.