Horizon Medical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980171 | DERMASENSE PLUS DISPERSIVE ELECTRODE | GEI | 1998-02-27 | View |
| 510(k) | K944969 | STERI-LUB LUBRICATION GEL | KMJ | 1995-02-27 | View |
| 510(k) | K883576 | HORIZON ORTHOPEDIC PIN PROTECTOR | LYT | 1988-09-30 | View |
No matching devices.
Advertisement