Prism Enterprises, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K030283 | BABY POD | April 22, 2003 |
| K020447 | MITYVAC MERLIN, MODEL 10027 | April 12, 2002 |
| K011532 | MITYVAC | July 30, 2001 |
| K000444 | MITYVIEW 4-WAY LATERAL EXPANDER SPECULUM | April 21, 2000 |