Mego Afek AC , Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Mego Afek AC , Ltd. has 17 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.
Last cleared in 2022. Active since 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mego Afek AC , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mego Afek AC , Ltd.
17 devices
Cleared
Apr 14, 2022
Amputee Garment for use with Lympha Press Optimal Plus
Cardiovascular
108d
Cleared
May 15, 2019
Recovery Pump, 737R (RPX)
Physical Medicine
76d
Cleared
Mar 25, 2019
Ballancer Gold, 1212
Physical Medicine
81d
Cleared
Feb 27, 2019
Lympha Press Optimal Plus
Cardiovascular
216d
Cleared
Nov 03, 2017
Phlebo Press DVT Model
Cardiovascular
98d
Cleared
May 31, 2017
Lympha Press Optimal Plus
Cardiovascular
89d
Cleared
Jan 27, 2017
RP Lite 760R
Physical Medicine
67d
Cleared
May 26, 2015
Ballancer 505 System, Model 1201-AC
Physical Medicine
111d
Cleared
Dec 16, 2014
Phlebo Press DVT 603
Cardiovascular
82d
Cleared
Jun 16, 2014
RECOVERY PUMP 737R
Physical Medicine
108d
Cleared
Jun 10, 2014
PCD 737A
Cardiovascular
90d
Cleared
Nov 01, 2013
PETITE BASIC SYSTEM 701 ELT
Cardiovascular
169d