Bühlmann Laboratories AG
Bühlmann Laboratories AG 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 February 6, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K232057 | BÜHLMANN fCAL® turbo and CALEX® Cap | February 6, 2024 |