Biocore Medical Technologies, 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 |
|---|
| K022995 | COLLATEK HYDROGEL | December 2, 2002 |
| K012995 | COLLATEK SHEET | October 25, 2001 |
| K012997 | COLLATEK FOAM | October 25, 2001 |
| K012990 | COLLATEK POWDER | October 24, 2001 |