Medical Device Manufacturer · US , Miami , FL

Magna Advanced Technologies, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1998
7
Total
7
Cleared
0
Denied

Magna Advanced Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 7 cleared submissions from 1998 to 1999. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Magna Advanced Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Magna Advanced Technologies, Inc.
7 devices
1-7 of 7
Filters