Cleveland Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K063872 | KINESIA | April 6, 2007 |
| K042039 | FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120 | November 17, 2004 |
| K013863 | CRYSTAL MONITOR MODEL 16 | February 19, 2002 |
| K001110 | CRYSTAL-EEG MODEL 15 | July 5, 2000 |
| K970672 | CRYSTAL-EEG MODEL 10 (MODEL 10) | May 22, 1997 |
| K964690 | LIBERTY VALVE | March 21, 1997 |
| K962591 | FOOT WEIGHT ALARM | December 4, 1996 |
| K954670 | PRESSORE MONITOR | October 30, 1995 |