Medical Device Manufacturer · US , St. Paul , MN

Horizon Medical, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1988

Recent clearances: DERMASENSE PLUS DISPERSIVE ELECTRODE, STERI-LUB LUBRICATION GEL

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Horizon Medical, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Feb 27, 1998

DERMASENSE PLUS DISPERSIVE ELECTRODE

General & Plastic Surgery · 38d