Linde Medical Sensors AG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Linde Medical Sensors AG has 4 FDA 510(k) cleared medical devices. Based in Basel, CH.
Historical record: 4 cleared submissions from 1999 to 2005. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Linde Medical Sensors AG Filter by specialty or product code using the sidebar.
4 devices
Cleared
Mar 04, 2005
TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009
Anesthesiology
88d
Cleared
Aug 24, 2004
TOSCA PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM
Toxicology
397d
Cleared
May 04, 2001
MICROGAS 7650 TRANSCUTANEOUS MONITOR
Anesthesiology
134d
Cleared
May 21, 1999
MICROGAS 7650 TRANSCUTANEOUS MONITOR
Anesthesiology
8d