Dornoch Medical Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K190789 | IntelliCartTM System | April 24, 2019 |
| K172481 | IntelliCart System | September 14, 2017 |
| K162421 | IntelliCartTM System | December 21, 2016 |
| K133786 | DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL | March 21, 2014 |
| K123188 | DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MO | March 4, 2013 |
| K081047 | TRANSPOSAL ULTRA SYSTEMS | April 29, 2008 |