Medical Device Manufacturer · US , Eden Prairie , MN

Celleration - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2004

1

Total

0

Cleared

1

Denied

Celleration has 0 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.

Active since 2004. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Celleration Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Celleration

1 devices

1-1 of 1

Not Cleared Jun 25, 2004

CELLERATION MIST THERAPY SYSTEM

DEN040004 · NRB

General & Plastic Surgery · 57d