Ron-Tech Medical , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K032585 | TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEM | January 9, 2004 |
| K992071 | TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE | August 27, 1999 |