Class Class II
Radial Artery Compression Tourniquets (K222182)
Description
Radial Artery Compression Tourniquets by Beijing Demax Medical Technology Co.,Ltd, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222182
Clearance Date2023-01-04
Clearance TypeTraditional
Product CodeDXC
Regulation Number870.4450
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222182
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. Radial Artery Compression Tourniquets (K222182) cites 0 predicate devices and is itself cited by 1 later device.
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232577 | Radial Compression Device | Ningbo Dizegens Medical Science Co.... | 2024 |
Trace the full predicate network for K222182
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.