Korr Medical Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K021490 | REEVUE INDIRECT CALORIMETER, MODEL#8100 | January 2, 2003 |
| K982995 | ACCUTRAX, MODEL EPF840 | December 4, 1998 |