Medical Device Manufacturer · US , Potomac , MD

Ad Rem Technology Sarl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Ad Rem Technology Sarl has 2 FDA 510(k) cleared medical devices. Based in Potomac, US.

Historical record: 2 cleared submissions from 2008 to 2015. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Ad Rem Technology Sarl Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ad Rem Technology Sarl

2 devices
1-2 of 2
Cleared Jun 16, 2015
VEINOPLUS SPORT NEUROMUSCULAR STIMULATOR
K141919 · NGX
Physical Medicine · 336d
Cleared Jan 30, 2008
VEINOPLUS NEUROMUSCULAR STIMULATOR
K072252 · IPF
Physical Medicine · 170d
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