Medical Device Manufacturer · US , Washington , DC

Mckenna & Cuneo - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1995

3

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mckenna & Cuneo Neurology ✕

1 devices

1-1 of 1

Cleared Sep 19, 1995

DANTEC KEYPOINT

Neurology · 369d