Linde Medical Sensors AG
Linde Medical Sensors AG has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Mar 4, 2005
Reviewing Linde Medical Sensors AG as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or get Linde Medical Sensors AG's full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 4 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| 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 |