Well Lead Medical Instruments
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K082815 | WELL LEAD SILICONE AND LATEX FOLEY CATHETERS | October 8, 2008 |
| K073383 | WELL LEAD REINFORCED ENDOTRACHEAL TUBE | July 10, 2008 |
| K042683 | WELL LEAD ENDOTRACHEAL TUBE | February 18, 2005 |
| K042684 | WELL LEAD TRACHEOSTOMY TUBE | February 17, 2005 |