Cutting Edge Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K963595 | SERAGARD VASCULAR ACCESS DEVICE | January 6, 1997 |
| K952606 | TARGETT PATCH | December 21, 1995 |