Schott Fiber Optics, 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 |
|---|
| K892390 | FLEXIBLE IMMERSIBLE HYSTEROSCOPE | February 2, 1990 |
| K892000 | FLEXIBLE IMMERSIBLE SIGMOIDOSCOPE | April 25, 1989 |