Durect Corp.
Durect Corp. appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 25, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K011383 | MICRODOSE CATH, MODELS 90121-201, -202, -203 | June 25, 2001 |