Intl. Medical Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K840384 | DIAGNOSTIC DILATATION & MENSTRUAL KIT | April 30, 1984 |
| K840381 | TAPERED CERVICAL DILATOR | April 30, 1984 |
| K840383 | MENSTRUAL ASPIRATION KIT | April 30, 1984 |
| K840382 | VACUUM ASPIRATION CATHETER | April 30, 1984 |
| K840380 | UTERINE SOUND | April 30, 1984 |