Linde Gas North America Llc
FDA Regulatory Profile
Linde Gas North America Llc appears in FDA public data with 1 recall, 1 510(k) clearance, 10 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1561-2013, Class II) was initiated on March 8, 2013. Its most recent 510(k) clearance was granted on March 18, 2011.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 10
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1561-2013 | Class II | MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen delivery system intended to | March 8, 2013 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K101792 | LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706 | March 18, 2011 |