Progressive Surgical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K982439 | PROXIDERM, MODELS TN 460, TN 90 460, BK 460 | September 8, 1998 |
| K970439 | PROXIDERM (D-460,D 90 460,D 180,460, PS 460) | April 16, 1997 |
| K942425 | PROXIDERM (TENTATIVE) | November 4, 1994 |