BeneVision Central Monitoring System (K242728)
Description
BeneVision Central Monitoring System by Shenzhen Mindray Bio-Medical Electronics Co., Ltd., an FDA 510(k) cleared cardiovascular device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242728
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. BeneVision Central Monitoring System (K242728) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K220058 | BeneVision Central Monitoring System | Shenzhen Mindray Bio-Medical Electr... | 2022 |
| K211900 | Patient Information Center iX | Philips Medizin Systeme Böblingen GmbH | 2022 |
| K161164 | CareEvent inclusive of the CareEvent Mobile Application acc... | Philips Medical Systems | 2016 |
Trace the full predicate network for K242728
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.