510(k) K110474 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
PHILIPS INTELLIVUE TCG10
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Sep 30, 2011 |
| Received | Feb 18, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K110474
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 16, 2015 | Philips Medical Systems, Inc. Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous.
The IntelliVue TcG10 is a device for the measurement of the transcutaneous O2 and CO2 partial pressure in neonates, pediatrics and adults Terminated |
LKD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.