510(k) K043357 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009
| Applicant | Linde Medical Sensors AG, Basel, CH |
| Decision | Substantially Equivalent, Mar 4, 2005 |
| Received | Dec 6, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043357
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.