Ursus Konsult AB
Ursus Konsult AB appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 18, 1979.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K792316 | TROTEX II SCREW NEEDLE BIOPSY INSTR. SET | December 18, 1979 |