510(k) K112652 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
SURESIGNS VS2+ -SURESIGNS VSI
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Oct 11, 2011 |
| Received | Sep 12, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112652
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 20, 2017 | Philips Electronics North America Corporation Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facility. Terminated |
MHX | None listed |
| Feb 14, 2013 | Philips Healthcare Inc. Philips Healthcare SureSigns VS2+
Model 863278 SureSigns VS2+ NBP and SpO2
Model 863279 SureSigns VS2+ NBP, SpO2 and Temperature
Product Usage:
The SureSigns VS2+ vital signs monitor is for monitorin Terminated |
DXN | None listed |
| Aug 30, 2012 | Philips Healthcare Inc. Philips SureSigns VSi/VS2+ patient monitors
Model Part Numbers
VSi/ 863275, 863276, 863277,
VS2+ 863278, 863279.
The SureSigns VS2+ vital signs monitor is for monitoring, recording and Terminated |
DXN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.