Lutech Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K170446 | LT-300 SD Digital Video Colposcope | May 21, 2017 |
| K160380 | LT-300 HD | May 13, 2016 |
| K150691 | Datalys Multi-Parameter Patient Monitor | May 15, 2015 |
| K143119 | LT-300 Video Colposcope | December 18, 2014 |