# Linde Medical Sensors AG

- Location (FDA's records): Basel, CH
- FDA decisions: 4 (1999–2005): 4 510(k) clearances
- Product codes: KLK (2), LKD (1), DOA (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kontron Instruments, Inc.: 1 (https://510kreport.com/company/kontron-instruments)

## Firms that cite its devices most
- Sentec AG: 2 (https://510kreport.com/company/sentec)
- Radiometer Medical Aps: 1 (https://510kreport.com/company/radiometer-medical)
- Radiometer Basel AG: 1 (https://510kreport.com/company/radiometer-basel)

## Its most-cited devices
- K991644: Microgas 7650 Transcutaneous Monitor (1999), cited by 2
- K003943: Microgas 7650 Transcutaneous Monitor (2001), cited by 2
- K043357: Tosca 500 PCO2, SPO2 and Pulse Rate Monitoring System, Model 5202009 (2005), cited by 1
- K032291: Tosca PCO2, SPO2 and Pulse Rate Monitoring System (2004), cited by 1

## Recent decisions
- K043357: Tosca 500 PCO2, SPO2 and Pulse Rate Monitoring System, Model 5202009 (Mar 4, 2005)
- K032291: Tosca PCO2, SPO2 and Pulse Rate Monitoring System (Aug 24, 2004)
- K003943: Microgas 7650 Transcutaneous Monitor (May 4, 2001)
- K991644: Microgas 7650 Transcutaneous Monitor (May 21, 1999)

Source page: https://510kreport.com/company/linde-medical-sensors