Progressive Surgical Products, Inc. is one of 7882 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Progressive Surgical Products, Inc. has 3 FDA 510(k) cleared medical devices. Based in Westbury, US.
Historical record: 3 cleared submissions from 1994 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Progressive Surgical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Progressive Surgical Products, Inc.
3 devices