Linde Medical Sensors AG

FDA Regulatory Profile

Linde Medical Sensors AG appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 4, 2005.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K043357TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009March 4, 2005
K032291TOSCA PCO2, SPO2 AND PULSE RATE MONITORING SYSTEMAugust 24, 2004
K003943MICROGAS 7650 TRANSCUTANEOUS MONITORMay 4, 2001
K991644MICROGAS 7650 TRANSCUTANEOUS MONITORMay 21, 1999