Ameco Medical Industries
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K152819 | Amecath Peripheral inserted Central Venous Catheter Sets | February 5, 2016 |
| K131144 | AMECO SHEATH INTRODUCER | August 15, 2013 |
| K131814 | AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER | July 26, 2013 |
| K123943 | AMECATH DUAL LUMEN HEMODIALYSIS CATHETER | April 2, 2013 |
| K110794 | AMECATH CVC AND AMECATH PRESSURE CVC SHORT TERM SINGLE AND MULTI-LUMEN CATHERIZATION KITS | December 21, 2011 |
| K110793 | AMECATH AND AMECATH UNIQATH SOFT SHORT TERM DUAL HEMODIALYSIS CATHETERIZATION KITS | December 16, 2011 |