Accutech Medical 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 |
|---|
| K090281 | ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES | March 4, 2009 |
| K061025 | ACCUTECH ENDOLITE PROBE | May 31, 2006 |