Medical Device Manufacturer · US , Walker , MN

Cytomedix - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cytomedix Hematology ✕

1 devices

1-1 of 1

Cleared Apr 11, 2003

AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129)

Hematology · 70d