Perstorp AB C/O Robert Joel Slomoff
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K905069 | IODOSORB GEL | January 31, 1991 |
| K870559 | IODOSORB POWDER | March 20, 1987 |