Althin Medical AB
Althin Medical AB appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 18, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K992564 | AF-180 HEMODIALYZER | January 18, 2000 |
| K992573 | AF-220 HEMODIALYZER | January 18, 2000 |
| K992563 | A-22 HEMODIALYZER | January 18, 2000 |
| K992566 | AF-150 HEMODIALYZER | January 18, 2000 |
| K992594 | A-15 HEMODIALYZER | September 24, 1999 |
| K992565 | A-18 HEMODIALYZER | September 23, 1999 |
| K990010 | ALTHIN MEDICAL AB ALTRACART II | April 15, 1999 |