Medical Device Manufacturer · US , Hopkonton , MA

Hemedex Incorporated - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2002

Recent clearances: QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT, HEMEDEX FIXATION DEVICE, HEMEDEX CRANIAL BOLT MODELS, 3601, 3602

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hemedex Incorporated Cardiovascular ✕

1 devices

1-1 of 1

Cleared May 08, 2002

QFLOW 500 PERFUSION MONITORING SYSTEM

Cardiovascular · 209d