Cerner CareAware Event Management
FDA 510(k) K151672 · Cerner Corporation
510(k) numberK151672
Submission
- Device name
- Cerner CareAware Event Management
- Applicant
- Cerner Corporation
Kansas City, MO, US - Received
- June 22, 2015
- Decision date
- December 21, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- MSX – System, Network And Communication, Physiological Monitors
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2300
- Specialty
- Cardiovascular
- Life-sustaining
- Yes
Other 510(k)s with product code MSX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261287 | Digistat CareMSX · Traditional | Ascom Ums Srl Unipersonale | 09/12/2026SE |
| K260211 | Dashboard (P007000)MSX · Traditional | Hill-Rom, Inc. | 08/13/2026SE |
| K261367 | Corsano CardioWatch 287-2 SystemMSX · Traditional | Corsano Health B.V. | 07/26/2026SE |
| K253654 | IntelliVue Measurement Rack 6000 (867317)MSX · Traditional | Philips Medizin Systeme Böblingen GmbH | 03/30/2026SE |
| K243270 | TigerConnect Alarm ManagementMSX · Traditional | Tigerconnect | 09/30/2025SE |
| K242728 | BeneVision Central Monitoring SystemMSX · Traditional | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 07/31/2025SE |
| K242750 | Central StationMSX · Traditional | Nihon Kohden Digital Health Solutions, LLC | 06/05/2025SE |
| K242842 | ANNE View, Central HubMSX · Traditional | Sibel Health, Inc. | 01/08/2025SE |
| K241397 | HinscopeMSX · Traditional | Hinlab Sas | 11/14/2024SE |
| K233834 | Infinity Gateway SuiteMSX · Traditional | Draeger Medical Systems, Inc. | 07/12/2024SE |
More from Draeger Medical Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K121758 | Cerner FETALINK+(VERSION1.0)HGM · Traditional | 10/09/2012SE |
| K093134 | Cerner Careaware IbusDRG · Traditional | 11/27/2009SE |
| K091251 | Cerner Fetalink (Version 1.0)HGM · Traditional | 08/25/2009SE |
| K091032 | Cerner Provision Workstation (Version 2.5)LLZ · Traditional | 06/22/2009SE |
| K070394 | Cerner Provision WorkstationLLZ · Traditional | 03/27/2007SE |
| K000770 | Proview Medical Image Display ModuleLLZ · Traditional | 05/16/2000SE |
| K955000 | Remote Viewing System Medical Image Display ModuleLMD · Traditional | 01/26/1996SE |
Questions and answers
When was Cerner CareAware Event Management cleared by the FDA?
Cerner CareAware Event Management (K151672) received a 510(k) decision of Substantially Equivalent on December 21, 2015, 182 days after the submission was received.
What is the product code of K151672?
The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.