Automated Medical Products Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K942910 | DEEPVISON | July 21, 1995 |
| K942818 | DEEP SUTURE | August 25, 1994 |
| K942002 | RETRACTOR | May 17, 1994 |
| K940199 | DISSECTOR | March 30, 1994 |
| K832827 | CORPULS 300 | November 3, 1983 |
| K792145 | AUTOMATIC RETRACTOR HOLDERS | December 5, 1979 |