Medical Device Manufacturer · US , Boulder , CO

Hei, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Recent clearances: HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hei, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Mar 21, 2012

HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

General Hospital · 538d