Insight Technologies Instruments, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K984537 | KERATOME SYSTEM, MODEL K3000 | May 14, 1999 |
| K974243 | KERATOME SYSTEM | January 20, 1998 |