Medical Device Manufacturer · DE , Pullach

Adeor Medical Technologies GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Recent clearances: MERIDIAN CRANIAL PERFORATOR

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Adeor Medical Technologies GmbH Neurology ✕

1 devices

1-1 of 1

Cleared Jul 17, 2012

MERIDIAN CRANIAL PERFORATOR

Neurology · 83d