Magna Advanced Technologies, Inc. - FDA 510(k) Cleared Devices
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.
7 devices
Cleared
Aug 19, 1999
MAGNATEK 30
Anesthesiology
84d
Cleared
Oct 02, 1998
MAGNATEK 40
Anesthesiology
45d
Cleared
Sep 22, 1998
MAGNATEK80
Anesthesiology
18d
Cleared
Sep 18, 1998
MTEK-1400
Anesthesiology
37d
Cleared
Sep 17, 1998
MTEK-1000
Anesthesiology
69d
Cleared
Jul 09, 1998
MAGNATEK C-300
General & Plastic Surgery
90d
Cleared
Jun 24, 1998
MAGNATEK ELECTROSURGICAL UNITS MODELS, ESU-10, ESU-15
General & Plastic Surgery
65d