Medical Device Manufacturer · US , Mosely , VA

Aframe Digital, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Recent clearances: MOBILECARE MONITOR, MOBILECARE MONITOR, MODEL 2100

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aframe Digital, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Apr 24, 2009

MOBILECARE MONITOR, MODEL 2100

General Hospital · 93d