Linde Medical Sensors AG
Basel, CH
Linde Medical Sensors AG appears in FDA device records in Basel, CH. FDA records list 4 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 4
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 4 510(k) clearances for Linde Medical Sensors AG between 1999 and 2005. The busiest year on record is 1999, with 1. The most recent is 2005, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1999 | 1 |
| 2001 | 1 |
| 2004 | 1 |
| 2005 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K043357 | TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009 | LKD | Substantially Equivalent | |
| K032291 | TOSCA PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM | DOA | Substantially Equivalent | |
| K003943 | MICROGAS 7650 TRANSCUTANEOUS MONITOR | KLK | Substantially Equivalent | |
| K991644 | MICROGAS 7650 TRANSCUTANEOUS MONITOR | KLK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain