Acotec Scientific Co., Ltd.
Acotec Scientific Co., Ltd. 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 Oct 7, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250688 | Cedar Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar Endovenous Radiofrequency Catheter (E | Oct 7, 2025 |