Cmt Medical Technologies, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K202235 | ArtPIX DRF | September 3, 2020 |
| K162224 | ArtPix Mobile EZ2GO | September 22, 2016 |
| K110849 | PRESTODR 4143 | April 26, 2011 |
| K103038 | DUET DRF | March 29, 2011 |
| K100400 | PRESTODR PORTABLE | April 22, 2010 |
| K080890 | SMARTSPOT PRIMAX | April 29, 2008 |
| K003438 | SMART RAD | July 3, 2001 |
| K001111 | PANORET, MODEL 1000A | July 7, 2000 |
| K991578 | SMARTSPOT 2000 | June 3, 1999 |
| K961140 | FLUOROPLUS CARDIAC TV | September 20, 1996 |
| K961307 | SMART SPOT | July 1, 1996 |
| K953950 | FLUORO CATHETER | September 18, 1995 |