Progressive Surgical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROXIDERM, MODELS TN 460, TN 90 460, BK 460, PROXIDERM (D-460,D 90 460,D 180,460, PS 460)
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Progressive Surgical Products, Inc. General & Plastic Surgery ✕
3 devices