American Medical Sales, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K052537 | CATELLA DIAGNOSTIC WORKSTATION, VERSION 4.0 | November 16, 2005 |
| K930230 | RADIOGRAPHIC WALL-MOUNTED CASSETTE HOLDER | April 27, 1993 |
| K922079 | ROTOLUX, SELECTOLUX, SHUTTERVUE | June 16, 1992 |