The Laryngeal Mask Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K130304 | LMA FAMILY OF AIRWAYS | May 30, 2014 |
| K062475 | LMA STONEBREAKER DEVICE; PROBE SIZE 1.0MM, 1.6MM, 2.0MM | May 9, 2007 |
| K051993 | LMA FASTRACH ETT SINGLE USE | December 13, 2005 |
| K991580 | ILM ENDOTRACHEAL TUBE | February 4, 2000 |