Eris Medical Technology
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K882295 | FILLING VOLUME OPTION | September 13, 1988 |
| K881878 | CATHETER WITHDRAWAL UNIT | July 28, 1988 |
| K850169 | ERIS URO-DIAGNOSTIC SYSTEM | April 22, 1985 |