Medelec , Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Medelec , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Surrey, England Gu22 9ju, GB.
Historical record: 8 cleared submissions from 1992 to 1997. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medelec , Ltd. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Jun 20, 1997
TECA. MILLENNIUM
Neurology
184d
Cleared
Jan 27, 1997
DG NERVUS
Neurology
91d
Cleared
Jan 17, 1996
DG PORTABLE SYSTEM
Neurology
134d
Cleared
Nov 08, 1995
DG EXAMINER PLUS
Neurology
86d
Cleared
Oct 19, 1995
TECA PREMIERE
Neurology
80d
Cleared
May 25, 1994
DG 3P SYSTEM
Neurology
238d
Cleared
Apr 26, 1994
ARC
Anesthesiology
209d
Cleared
Nov 24, 1992
SAPPHIRE PREMIERE
Neurology
141d